Canonical Allele Identifier: CA1683032301

Gene: MAD1L1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2225273_2225274delinsAG , CM000669.2:g.2225273_2225274delinsAG	GRCh38
NC_000007.13:g.2264908_2264909delinsAG , CM000669.1:g.2264908_2264909delinsAG	GRCh37
NC_000007.12:g.2231434_2231435delinsAG	NCBI36
NG_011518.1:g.12675_12676delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265854.12:c.291+136_291+137delinsCT MANE Select	ENSP00000265854.7:n.291+136_291+137delinsCT
ENST00000651235.1:c.*2699+136_*2699+137delinsCT	ENSP00000498895.1:n.*2699+136_*2699+137delinsCT
ENST00000265854.11:c.291+136_291+137delinsCT	ENSP00000265854.7:n.291+136_291+137delinsCT
ENST00000399654.6:c.291+136_291+137delinsCT	ENSP00000382562.2:n.291+136_291+137delinsCT
ENST00000402746.5:c.-124-2520_-124-2519delinsCT	ENSP00000384155.1:n.-124-2520_-124-2519delinsCT
ENST00000406869.5:c.291+136_291+137delinsCT	ENSP00000385334.1:n.291+136_291+137delinsCT
ENST00000429625.5:c.78+136_78+137delinsCT	ENSP00000413139.1:n.78+136_78+137delinsCT
ENST00000429779.1:c.291+136_291+137delinsCT	ENSP00000395457.1:n.291+136_291+137delinsCT
ENST00000455998.5:c.151-2520_151-2519delinsCT	ENSP00000390099.1:n.151-2520_151-2519delinsCT
NM_001013836.1:c.291+136_291+137delinsCT	NP_001013858.1:n.291+136_291+137delinsCT
NM_001013837.1:c.291+136_291+137delinsCT	NP_001013859.1:n.291+136_291+137delinsCT
NM_001304523.1:c.291+136_291+137delinsCT	NP_001291452.1:n.291+136_291+137delinsCT
NM_001304524.1:c.-124-2520_-124-2519delinsCT	NP_001291453.1:n.-124-2520_-124-2519delinsCT
NM_003550.2:c.291+136_291+137delinsCT	NP_003541.2:n.291+136_291+137delinsCT
XM_005249877.1:c.151-2520_151-2519delinsCT	XP_005249934.1:n.151-2520_151-2519delinsCT
XM_011515567.1:c.291+136_291+137delinsCT	XP_011513869.1:n.291+136_291+137delinsCT
XM_011515568.1:c.291+136_291+137delinsCT	XP_011513870.1:n.291+136_291+137delinsCT
XM_011515570.1:c.291+136_291+137delinsCT	XP_011513872.1:n.291+136_291+137delinsCT
XM_011515568.3:c.291+136_291+137delinsCT	XP_011513870.1:n.291+136_291+137delinsCT
XM_017012690.1:c.483+136_483+137delinsCT	XP_016868179.1:n.483+136_483+137delinsCT
XM_024446951.1:c.291+136_291+137delinsCT	XP_024302719.1:n.291+136_291+137delinsCT
XM_024446952.1:c.291+136_291+137delinsCT	XP_024302720.1:n.291+136_291+137delinsCT
NM_001013836.2:c.291+136_291+137delinsCT MANE Select	NP_001013858.1:n.291+136_291+137delinsCT
NM_001013837.2:c.291+136_291+137delinsCT	NP_001013859.1:n.291+136_291+137delinsCT
NM_001304523.2:c.291+136_291+137delinsCT	NP_001291452.1:n.291+136_291+137delinsCT
NM_001304524.2:c.-124-2520_-124-2519delinsCT	NP_001291453.1:n.-124-2520_-124-2519delinsCT
NM_003550.3:c.291+136_291+137delinsCT	NP_003541.2:n.291+136_291+137delinsCT