Canonical Allele Identifier: CA478131837

Gene: GAPDH

Linked Data

• MyVariant Identifiers: chr12:g.6644019A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534853A>G , CM000674.2:g.6534853A>G	GRCh38
NC_000012.11:g.6644019A>G , CM000674.1:g.6644019A>G	GRCh37
NC_000012.10:g.6514280A>G	NCBI36
NG_007073.2:g.5363A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.21A>G MANE Select	ENSP00000229239.5:p.Gly7=
ENST00000229239.9:c.21A>G	ENSP00000229239.5:p.Gly7=
ENST00000396856.5:c.-232A>G	ENSP00000380065.1:n.-232A>G
ENST00000396859.5:c.21A>G	ENSP00000380068.1:p.Gly7=
ENST00000396861.5:c.21A>G	ENSP00000380070.1:p.Gly7=
ENST00000466525.1:n.62A>G
ENST00000466588.5:n.100A>G
ENST00000474249.5:n.73A>G
ENST00000492719.5:n.81A>G
ENST00000496049.1:n.102A>G
NM_001289745.1:c.21A>G	NP_001276674.1:p.Gly7=
NM_001289746.1:c.21A>G	NP_001276675.1:p.Gly7=
NM_002046.5:c.21A>G	NP_002037.2:p.Gly7=
NM_001289745.2:c.21A>G	NP_001276674.1:p.Gly7=
NM_001357943.1:c.21A>G	NP_001344872.1:p.Gly7=
NM_002046.6:c.21A>G	NP_002037.2:p.Gly7=
NR_152150.1:n.97A>G
NM_002046.7:c.21A>G MANE Select	NP_002037.2:p.Gly7=
NM_001289745.3:c.21A>G	NP_001276674.1:p.Gly7=
NM_001289746.2:c.21A>G	NP_001276675.1:p.Gly7=
NM_001357943.2:c.21A>G	NP_001344872.1:p.Gly7=
NR_152150.2:n.97A>G