Canonical Allele Identifier: CA6409380

Gene: GAPDH

Linked Data

• dbSNP Id: rs749762041
• ExAC: 12:6644018 G / C
• gnomAD v2: 12-6644018-G-C
• gnomAD v4: 12-6534852-G-C
• MyVariant Identifiers: chr12:g.6644018G>C (hg19) ; chr12:g.6534852G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534852G>C , CM000674.2:g.6534852G>C	GRCh38
NC_000012.11:g.6644018G>C , CM000674.1:g.6644018G>C	GRCh37
NC_000012.10:g.6514279G>C	NCBI36
NG_007073.2:g.5362G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.20G>C MANE Select	ENSP00000229239.5:p.Gly7Ala
ENST00000229239.9:c.20G>C	ENSP00000229239.5:p.Gly7Ala
ENST00000396856.5:c.-233G>C	ENSP00000380065.1:n.-233G>C
ENST00000396859.5:c.20G>C	ENSP00000380068.1:p.Gly7Ala
ENST00000396861.5:c.20G>C	ENSP00000380070.1:p.Gly7Ala
ENST00000466525.1:n.61G>C
ENST00000466588.5:n.99G>C
ENST00000474249.5:n.72G>C
ENST00000492719.5:n.80G>C
ENST00000496049.1:n.101G>C
NM_001289745.1:c.20G>C	NP_001276674.1:p.Gly7Ala
NM_001289746.1:c.20G>C	NP_001276675.1:p.Gly7Ala
NM_002046.5:c.20G>C	NP_002037.2:p.Gly7Ala
NM_001289745.2:c.20G>C	NP_001276674.1:p.Gly7Ala
NM_001357943.1:c.20G>C	NP_001344872.1:p.Gly7Ala
NM_002046.6:c.20G>C	NP_002037.2:p.Gly7Ala
NR_152150.1:n.96G>C
NM_002046.7:c.20G>C MANE Select	NP_002037.2:p.Gly7Ala
NM_001289745.3:c.20G>C	NP_001276674.1:p.Gly7Ala
NM_001289746.2:c.20G>C	NP_001276675.1:p.Gly7Ala
NM_001357943.2:c.20G>C	NP_001344872.1:p.Gly7Ala
NR_152150.2:n.96G>C