Canonical Allele Identifier: CA572153241

Gene: MAD1L1

Linked Data

• dbSNP Id: rs1318098203
• gnomAD v2: 7-2264882-CCCAGGGA-C
• gnomAD v3: 7-2225247-CCCAGGGA-C
• gnomAD v4: 7-2225247-CCCAGGGA-C
• MyVariant Identifiers: chr7:g.2264883_2264889del (hg19) ; chr7:g.2225248_2225254del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.2225249_2225255del , CM000669.2:g.2225249_2225255del	GRCh38
NC_000007.13:g.2264884_2264890del , CM000669.1:g.2264884_2264890del	GRCh37
NC_000007.12:g.2231410_2231416del	NCBI36
NG_011518.1:g.12695_12701del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265854.12:c.291+156_291+162del MANE Select	ENSP00000265854.7:n.291+156_291+162del
ENST00000651235.1:c.*2699+156_*2699+162del	ENSP00000498895.1:n.*2699+156_*2699+162del
ENST00000265854.11:c.291+156_291+162del	ENSP00000265854.7:n.291+156_291+162del
ENST00000399654.6:c.291+156_291+162del	ENSP00000382562.2:n.291+156_291+162del
ENST00000402746.5:c.-124-2500_-124-2494del	ENSP00000384155.1:n.-124-2500_-124-2494del
ENST00000406869.5:c.291+156_291+162del	ENSP00000385334.1:n.291+156_291+162del
ENST00000429625.5:c.78+156_78+162del	ENSP00000413139.1:n.78+156_78+162del
ENST00000429779.1:c.291+156_291+162del	ENSP00000395457.1:n.291+156_291+162del
ENST00000455998.5:c.151-2500_151-2494del	ENSP00000390099.1:n.151-2500_151-2494del
NM_001013836.1:c.291+156_291+162del	NP_001013858.1:n.291+156_291+162del
NM_001013837.1:c.291+156_291+162del	NP_001013859.1:n.291+156_291+162del
NM_001304523.1:c.291+156_291+162del	NP_001291452.1:n.291+156_291+162del
NM_001304524.1:c.-124-2500_-124-2494del	NP_001291453.1:n.-124-2500_-124-2494del
NM_003550.2:c.291+156_291+162del	NP_003541.2:n.291+156_291+162del
XM_005249877.1:c.151-2500_151-2494del	XP_005249934.1:n.151-2500_151-2494del
XM_011515567.1:c.291+156_291+162del	XP_011513869.1:n.291+156_291+162del
XM_011515568.1:c.291+156_291+162del	XP_011513870.1:n.291+156_291+162del
XM_011515570.1:c.291+156_291+162del	XP_011513872.1:n.291+156_291+162del
XM_011515568.3:c.291+156_291+162del	XP_011513870.1:n.291+156_291+162del
XM_017012690.1:c.483+156_483+162del	XP_016868179.1:n.483+156_483+162del
XM_024446951.1:c.291+156_291+162del	XP_024302719.1:n.291+156_291+162del
XM_024446952.1:c.291+156_291+162del	XP_024302720.1:n.291+156_291+162del
NM_001013836.2:c.291+156_291+162del MANE Select	NP_001013858.1:n.291+156_291+162del
NM_001013837.2:c.291+156_291+162del	NP_001013859.1:n.291+156_291+162del
NM_001304523.2:c.291+156_291+162del	NP_001291452.1:n.291+156_291+162del
NM_001304524.2:c.-124-2500_-124-2494del	NP_001291453.1:n.-124-2500_-124-2494del
NM_003550.3:c.291+156_291+162del	NP_003541.2:n.291+156_291+162del