Canonical Allele Identifier: CA478131834

Gene: GAPDH

Linked Data

• MyVariant Identifiers: chr12:g.6644016C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534850C>G , CM000674.2:g.6534850C>G	GRCh38
NC_000012.11:g.6644016C>G , CM000674.1:g.6644016C>G	GRCh37
NC_000012.10:g.6514277C>G	NCBI36
NG_007073.2:g.5360C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.18C>G MANE Select	ENSP00000229239.5:p.Val6=
ENST00000229239.9:c.18C>G	ENSP00000229239.5:p.Val6=
ENST00000396856.5:c.-235C>G	ENSP00000380065.1:n.-235C>G
ENST00000396859.5:c.18C>G	ENSP00000380068.1:p.Val6=
ENST00000396861.5:c.18C>G	ENSP00000380070.1:p.Val6=
ENST00000466525.1:n.59C>G
ENST00000466588.5:n.97C>G
ENST00000474249.5:n.70C>G
ENST00000492719.5:n.78C>G
ENST00000496049.1:n.99C>G
NM_001289745.1:c.18C>G	NP_001276674.1:p.Val6=
NM_001289746.1:c.18C>G	NP_001276675.1:p.Val6=
NM_002046.5:c.18C>G	NP_002037.2:p.Val6=
NM_001289745.2:c.18C>G	NP_001276674.1:p.Val6=
NM_001357943.1:c.18C>G	NP_001344872.1:p.Val6=
NM_002046.6:c.18C>G	NP_002037.2:p.Val6=
NR_152150.1:n.94C>G
NM_002046.7:c.18C>G MANE Select	NP_002037.2:p.Val6=
NM_001289745.3:c.18C>G	NP_001276674.1:p.Val6=
NM_001289746.2:c.18C>G	NP_001276675.1:p.Val6=
NM_001357943.2:c.18C>G	NP_001344872.1:p.Val6=
NR_152150.2:n.94C>G