Canonical Allele Identifier: CA603118194

Gene: GAPDH

Linked Data

• dbSNP Id: rs1265734664
• gnomAD v2: 12-6643803-C-T
• gnomAD v3: 12-6534637-C-T
• gnomAD v4: 12-6534637-C-T
• MyVariant Identifiers: chr12:g.6643803C>T (hg19) ; chr12:g.6534637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534637C>T , CM000674.2:g.6534637C>T	GRCh38
NC_000012.11:g.6643803C>T , CM000674.1:g.6643803C>T	GRCh37
NC_000012.10:g.6514064C>T	NCBI36
NG_007073.2:g.5147C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+68C>T MANE Select	ENSP00000229239.5:n.-24+68C>T
ENST00000229239.9:c.-24+68C>T	ENSP00000229239.5:n.-24+68C>T
ENST00000396856.5:c.-276+68C>T	ENSP00000380065.1:n.-276+68C>T
ENST00000396861.5:c.-48C>T	ENSP00000380070.1:n.-48C>T
ENST00000474249.5:n.29+68C>T
ENST00000492719.5:n.37+68C>T
ENST00000496049.1:n.58+68C>T
NM_001289745.1:c.-48C>T	NP_001276674.1:n.-48C>T
NM_002046.5:c.-24+68C>T	NP_002037.2:n.-24+68C>T
NM_001289745.2:c.-48C>T	NP_001276674.1:n.-48C>T
NM_001357943.1:c.-24+68C>T	NP_001344872.1:n.-24+68C>T
NM_002046.6:c.-24+68C>T	NP_002037.2:n.-24+68C>T
NR_152150.1:n.53+68C>T
NM_002046.7:c.-24+68C>T MANE Select	NP_002037.2:n.-24+68C>T
NM_001289745.3:c.-48C>T	NP_001276674.1:n.-48C>T
NM_001289746.2:c.-196C>T	NP_001276675.1:n.-196C>T
NM_001357943.2:c.-24+68C>T	NP_001344872.1:n.-24+68C>T
NR_152150.2:n.53+68C>T