Canonical Allele Identifier: CA383602202

Gene: GAPDH

Linked Data

• MyVariant Identifiers: chr12:g.6644014G>T (hg19) ; chr12:g.6534848G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534848G>T , CM000674.2:g.6534848G>T	GRCh38
NC_000012.11:g.6644014G>T , CM000674.1:g.6644014G>T	GRCh37
NC_000012.10:g.6514275G>T	NCBI36
NG_007073.2:g.5358G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.16G>T MANE Select	ENSP00000229239.5:p.Val6Phe
ENST00000229239.9:c.16G>T	ENSP00000229239.5:p.Val6Phe
ENST00000396856.5:c.-237G>T	ENSP00000380065.1:n.-237G>T
ENST00000396859.5:c.16G>T	ENSP00000380068.1:p.Val6Phe
ENST00000396861.5:c.16G>T	ENSP00000380070.1:p.Val6Phe
ENST00000466525.1:n.57G>T
ENST00000466588.5:n.95G>T
ENST00000474249.5:n.68G>T
ENST00000492719.5:n.76G>T
ENST00000496049.1:n.97G>T
NM_001289745.1:c.16G>T	NP_001276674.1:p.Val6Phe
NM_001289746.1:c.16G>T	NP_001276675.1:p.Val6Phe
NM_002046.5:c.16G>T	NP_002037.2:p.Val6Phe
NM_001289745.2:c.16G>T	NP_001276674.1:p.Val6Phe
NM_001357943.1:c.16G>T	NP_001344872.1:p.Val6Phe
NM_002046.6:c.16G>T	NP_002037.2:p.Val6Phe
NR_152150.1:n.92G>T
NM_002046.7:c.16G>T MANE Select	NP_002037.2:p.Val6Phe
NM_001289745.3:c.16G>T	NP_001276674.1:p.Val6Phe
NM_001289746.2:c.16G>T	NP_001276675.1:p.Val6Phe
NM_001357943.2:c.16G>T	NP_001344872.1:p.Val6Phe
NR_152150.2:n.92G>T