Canonical Allele Identifier: CA690978439

Gene: GAPDH

Linked Data

• dbSNP Id: rs1484836975
• gnomAD v3: 12-6534642-T-C
• gnomAD v4: 12-6534642-T-C
• MyVariant Identifiers: chr12:g.6643808T>C (hg19) ; chr12:g.6534642T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534642T>C , CM000674.2:g.6534642T>C	GRCh38
NC_000012.11:g.6643808T>C , CM000674.1:g.6643808T>C	GRCh37
NC_000012.10:g.6514069T>C	NCBI36
NG_007073.2:g.5152T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+73T>C MANE Select	ENSP00000229239.5:n.-24+73T>C
ENST00000229239.9:c.-24+73T>C	ENSP00000229239.5:n.-24+73T>C
ENST00000396856.5:c.-276+73T>C	ENSP00000380065.1:n.-276+73T>C
ENST00000396861.5:c.-43T>C	ENSP00000380070.1:n.-43T>C
ENST00000474249.5:n.29+73T>C
ENST00000492719.5:n.37+73T>C
ENST00000496049.1:n.58+73T>C
NM_001289745.1:c.-43T>C	NP_001276674.1:n.-43T>C
NM_002046.5:c.-24+73T>C	NP_002037.2:n.-24+73T>C
NM_001289745.2:c.-43T>C	NP_001276674.1:n.-43T>C
NM_001357943.1:c.-24+73T>C	NP_001344872.1:n.-24+73T>C
NM_002046.6:c.-24+73T>C	NP_002037.2:n.-24+73T>C
NR_152150.1:n.53+73T>C
NM_002046.7:c.-24+73T>C MANE Select	NP_002037.2:n.-24+73T>C
NM_001289745.3:c.-43T>C	NP_001276674.1:n.-43T>C
NM_001289746.2:c.-191T>C	NP_001276675.1:n.-191T>C
NM_001357943.2:c.-24+73T>C	NP_001344872.1:n.-24+73T>C
NR_152150.2:n.53+73T>C