Canonical Allele Identifier: CA383602149

Gene: GAPDH

Linked Data

• MyVariant Identifiers: chr12:g.6644003G>C (hg19) ; chr12:g.6534837G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534837G>C , CM000674.2:g.6534837G>C	GRCh38
NC_000012.11:g.6644003G>C , CM000674.1:g.6644003G>C	GRCh37
NC_000012.10:g.6514264G>C	NCBI36
NG_007073.2:g.5347G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.5G>C MANE Select	ENSP00000229239.5:p.Gly2Ala
ENST00000229239.9:c.5G>C	ENSP00000229239.5:p.Gly2Ala
ENST00000396856.5:c.-248G>C	ENSP00000380065.1:n.-248G>C
ENST00000396859.5:c.5G>C	ENSP00000380068.1:p.Gly2Ala
ENST00000396861.5:c.5G>C	ENSP00000380070.1:p.Gly2Ala
ENST00000466525.1:n.46G>C
ENST00000466588.5:n.84G>C
ENST00000474249.5:n.57G>C
ENST00000492719.5:n.65G>C
ENST00000496049.1:n.86G>C
NM_001289745.1:c.5G>C	NP_001276674.1:p.Gly2Ala
NM_001289746.1:c.5G>C	NP_001276675.1:p.Gly2Ala
NM_002046.5:c.5G>C	NP_002037.2:p.Gly2Ala
NM_001289745.2:c.5G>C	NP_001276674.1:p.Gly2Ala
NM_001357943.1:c.5G>C	NP_001344872.1:p.Gly2Ala
NM_002046.6:c.5G>C	NP_002037.2:p.Gly2Ala
NR_152150.1:n.81G>C
NM_002046.7:c.5G>C MANE Select	NP_002037.2:p.Gly2Ala
NM_001289745.3:c.5G>C	NP_001276674.1:p.Gly2Ala
NM_001289746.2:c.5G>C	NP_001276675.1:p.Gly2Ala
NM_001357943.2:c.5G>C	NP_001344872.1:p.Gly2Ala
NR_152150.2:n.81G>C