Canonical Allele Identifier: CA383602122

Gene: GAPDH

Linked Data

• dbSNP Id: rs1946423165
• gnomAD v3: 12-6534833-A-G
• gnomAD v4: 12-6534833-A-G
• MyVariant Identifiers: chr12:g.6643999A>G (hg19) ; chr12:g.6534833A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534833A>G , CM000674.2:g.6534833A>G	GRCh38
NC_000012.11:g.6643999A>G , CM000674.1:g.6643999A>G	GRCh37
NC_000012.10:g.6514260A>G	NCBI36
NG_007073.2:g.5343A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.1A>G MANE Select	ENSP00000229239.5:p.Met1Val
ENST00000229239.9:c.1A>G	ENSP00000229239.5:p.Met1Val
ENST00000396856.5:c.-252A>G	ENSP00000380065.1:n.-252A>G
ENST00000396859.5:c.1A>G	ENSP00000380068.1:p.Met1Val
ENST00000396861.5:c.1A>G	ENSP00000380070.1:p.Met1Val
ENST00000466525.1:n.42A>G
ENST00000466588.5:n.80A>G
ENST00000474249.5:n.53A>G
ENST00000492719.5:n.61A>G
ENST00000496049.1:n.82A>G
NM_001289745.1:c.1A>G	NP_001276674.1:p.Met1Val
NM_001289746.1:c.1A>G	NP_001276675.1:p.Met1Val
NM_002046.5:c.1A>G	NP_002037.2:p.Met1Val
NM_001289745.2:c.1A>G	NP_001276674.1:p.Met1Val
NM_001357943.1:c.1A>G	NP_001344872.1:p.Met1Val
NM_002046.6:c.1A>G	NP_002037.2:p.Met1Val
NR_152150.1:n.77A>G
NM_002046.7:c.1A>G MANE Select	NP_002037.2:p.Met1Val
NM_001289745.3:c.1A>G	NP_001276674.1:p.Met1Val
NM_001289746.2:c.1A>G	NP_001276675.1:p.Met1Val
NM_001357943.2:c.1A>G	NP_001344872.1:p.Met1Val
NR_152150.2:n.77A>G