Canonical Allele Identifier: CA603118195

Gene: GAPDH

Linked Data

• dbSNP Id: rs1193480515
• gnomAD v2: 12-6643826-G-T
• gnomAD v3: 12-6534660-G-T
• gnomAD v4: 12-6534660-G-T
• MyVariant Identifiers: chr12:g.6643826G>T (hg19) ; chr12:g.6534660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534660G>T , CM000674.2:g.6534660G>T	GRCh38
NC_000012.11:g.6643826G>T , CM000674.1:g.6643826G>T	GRCh37
NC_000012.10:g.6514087G>T	NCBI36
NG_007073.2:g.5170G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+91G>T MANE Select	ENSP00000229239.5:n.-24+91G>T
ENST00000229239.9:c.-24+91G>T	ENSP00000229239.5:n.-24+91G>T
ENST00000396856.5:c.-276+91G>T	ENSP00000380065.1:n.-276+91G>T
ENST00000396861.5:c.-25G>T	ENSP00000380070.1:n.-25G>T
ENST00000474249.5:n.29+91G>T
ENST00000492719.5:n.37+91G>T
ENST00000496049.1:n.58+91G>T
NM_001289745.1:c.-25G>T	NP_001276674.1:n.-25G>T
NM_001289746.1:c.-173G>T	NP_001276675.1:n.-173G>T
NM_002046.5:c.-24+91G>T	NP_002037.2:n.-24+91G>T
NM_001289745.2:c.-25G>T	NP_001276674.1:n.-25G>T
NM_001357943.1:c.-24+91G>T	NP_001344872.1:n.-24+91G>T
NM_002046.6:c.-24+91G>T	NP_002037.2:n.-24+91G>T
NR_152150.1:n.53+91G>T
NM_002046.7:c.-24+91G>T MANE Select	NP_002037.2:n.-24+91G>T
NM_001289745.3:c.-25G>T	NP_001276674.1:n.-25G>T
NM_001289746.2:c.-173G>T	NP_001276675.1:n.-173G>T
NM_001357943.2:c.-24+91G>T	NP_001344872.1:n.-24+91G>T
NR_152150.2:n.53+91G>T