Canonical Allele Identifier: CA478131811

Gene: GAPDH

Linked Data

• dbSNP Id: rs2136066674
• MyVariant Identifiers: chr12:g.6644010G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534844G>A , CM000674.2:g.6534844G>A	GRCh38
NC_000012.11:g.6644010G>A , CM000674.1:g.6644010G>A	GRCh37
NC_000012.10:g.6514271G>A	NCBI36
NG_007073.2:g.5354G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.12G>A MANE Select	ENSP00000229239.5:p.Val4=
ENST00000229239.9:c.12G>A	ENSP00000229239.5:p.Val4=
ENST00000396856.5:c.-241G>A	ENSP00000380065.1:n.-241G>A
ENST00000396859.5:c.12G>A	ENSP00000380068.1:p.Val4=
ENST00000396861.5:c.12G>A	ENSP00000380070.1:p.Val4=
ENST00000466525.1:n.53G>A
ENST00000466588.5:n.91G>A
ENST00000474249.5:n.64G>A
ENST00000492719.5:n.72G>A
ENST00000496049.1:n.93G>A
NM_001289745.1:c.12G>A	NP_001276674.1:p.Val4=
NM_001289746.1:c.12G>A	NP_001276675.1:p.Val4=
NM_002046.5:c.12G>A	NP_002037.2:p.Val4=
NM_001289745.2:c.12G>A	NP_001276674.1:p.Val4=
NM_001357943.1:c.12G>A	NP_001344872.1:p.Val4=
NM_002046.6:c.12G>A	NP_002037.2:p.Val4=
NR_152150.1:n.88G>A
NM_002046.7:c.12G>A MANE Select	NP_002037.2:p.Val4=
NM_001289745.3:c.12G>A	NP_001276674.1:p.Val4=
NM_001289746.2:c.12G>A	NP_001276675.1:p.Val4=
NM_001357943.2:c.12G>A	NP_001344872.1:p.Val4=
NR_152150.2:n.88G>A