Canonical Allele Identifier: CA572153249
Gene: MAD1L1 HGNC NCBI

Linked Data

dbSNP Id: rs1562389647

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.2225274_2225275insGTACCGTGCACAGCCCCCTTGCTCCCAGGGACTAGGATGTGATTTCTTATA , CM000669.2:g.2225274_2225275insGTACCGTGCACAGCCCCCTTGCTCCCAGGGACTAGGATGTGATTTCTTATA GRCh38
NC_000007.13:g.2264909_2264910insGTACCGTGCACAGCCCCCTTGCTCCCAGGGACTAGGATGTGATTTCTTATA , CM000669.1:g.2264909_2264910insGTACCGTGCACAGCCCCCTTGCTCCCAGGGACTAGGATGTGATTTCTTATA GRCh37
NC_000007.12:g.2231435_2231436insGTACCGTGCACAGCCCCCTTGCTCCCAGGGACTAGGATGTGATTTCTTATA NCBI36
NG_011518.1:g.12674_12675insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265854.12:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC MANE Select ENSP00000265854.7:n.291+135_291+136insTATAAGAAATCACATCCTAGTCC...
ENST00000651235.1:c.*2699+135_*2699+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000498895.1:n.*2699+135_*2699+136insTATAAGAAATCACATCCTA...
ENST00000265854.11:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000265854.7:n.291+135_291+136insTATAAGAAATCACATCCTAGTCC...
ENST00000399654.6:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000382562.2:n.291+135_291+136insTATAAGAAATCACATCCTAGTCC...
ENST00000402746.5:c.-124-2521_-124-2520insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000384155.1:n.-124-2521_-124-2520insTATAAGAAATCACATCCTA...
ENST00000406869.5:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000385334.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCC...
ENST00000429625.5:c.78+135_78+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000413139.1:n.78+135_78+136insTATAAGAAATCACATCCTAGTCCCT...
ENST00000429779.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000395457.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCC...
ENST00000455998.5:c.151-2521_151-2520insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC ENSP00000390099.1:n.151-2521_151-2520insTATAAGAAATCACATCCTAGT...
NM_001013836.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001013858.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001013837.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001013859.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001304523.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001291452.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001304524.1:c.-124-2521_-124-2520insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001291453.1:n.-124-2521_-124-2520insTATAAGAAATCACATCCTAGTC...
NM_003550.2:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_003541.2:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGA...
XM_005249877.1:c.151-2521_151-2520insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_005249934.1:n.151-2521_151-2520insTATAAGAAATCACATCCTAGTCCC...
XM_011515567.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_011513869.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_011515568.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_011513870.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_011515570.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_011513872.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_011515568.3:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_011513870.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_017012690.1:c.483+135_483+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_016868179.1:n.483+135_483+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_024446951.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_024302719.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
XM_024446952.1:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC XP_024302720.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001013836.2:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC MANE Select NP_001013858.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001013837.2:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001013859.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001304523.2:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001291452.1:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTG...
NM_001304524.2:c.-124-2521_-124-2520insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_001291453.1:n.-124-2521_-124-2520insTATAAGAAATCACATCCTAGTC...
NM_003550.3:c.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGAGCAAGGGGGCTGTGCACGGTAC NP_003541.2:n.291+135_291+136insTATAAGAAATCACATCCTAGTCCCTGGGA...