Canonical Allele Identifier: CA6409376

Gene: GAPDH

Linked Data

• dbSNP Id: rs367765818
• ExAC: 12:6644008 G / A
• gnomAD v2: 12-6644008-G-A
• gnomAD v3: 12-6534842-G-A
• gnomAD v4: 12-6534842-G-A
• MyVariant Identifiers: chr12:g.6644008G>A (hg19) ; chr12:g.6534842G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534842G>A , CM000674.2:g.6534842G>A	GRCh38
NC_000012.11:g.6644008G>A , CM000674.1:g.6644008G>A	GRCh37
NC_000012.10:g.6514269G>A	NCBI36
NG_007073.2:g.5352G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.10G>A MANE Select	ENSP00000229239.5:p.Val4Met
ENST00000229239.9:c.10G>A	ENSP00000229239.5:p.Val4Met
ENST00000396856.5:c.-243G>A	ENSP00000380065.1:n.-243G>A
ENST00000396859.5:c.10G>A	ENSP00000380068.1:p.Val4Met
ENST00000396861.5:c.10G>A	ENSP00000380070.1:p.Val4Met
ENST00000466525.1:n.51G>A
ENST00000466588.5:n.89G>A
ENST00000474249.5:n.62G>A
ENST00000492719.5:n.70G>A
ENST00000496049.1:n.91G>A
NM_001289745.1:c.10G>A	NP_001276674.1:p.Val4Met
NM_001289746.1:c.10G>A	NP_001276675.1:p.Val4Met
NM_002046.5:c.10G>A	NP_002037.2:p.Val4Met
NM_001289745.2:c.10G>A	NP_001276674.1:p.Val4Met
NM_001357943.1:c.10G>A	NP_001344872.1:p.Val4Met
NM_002046.6:c.10G>A	NP_002037.2:p.Val4Met
NR_152150.1:n.86G>A
NM_002046.7:c.10G>A MANE Select	NP_002037.2:p.Val4Met
NM_001289745.3:c.10G>A	NP_001276674.1:p.Val4Met
NM_001289746.2:c.10G>A	NP_001276675.1:p.Val4Met
NM_001357943.2:c.10G>A	NP_001344872.1:p.Val4Met
NR_152150.2:n.86G>A