Canonical Allele Identifier: CA383602163

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534840-A-T
• MyVariant Identifiers: chr12:g.6644006A>T (hg19) ; chr12:g.6534840A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534840A>T , CM000674.2:g.6534840A>T	GRCh38
NC_000012.11:g.6644006A>T , CM000674.1:g.6644006A>T	GRCh37
NC_000012.10:g.6514267A>T	NCBI36
NG_007073.2:g.5350A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.8A>T MANE Select	ENSP00000229239.5:p.Lys3Met
ENST00000229239.9:c.8A>T	ENSP00000229239.5:p.Lys3Met
ENST00000396856.5:c.-245A>T	ENSP00000380065.1:n.-245A>T
ENST00000396859.5:c.8A>T	ENSP00000380068.1:p.Lys3Met
ENST00000396861.5:c.8A>T	ENSP00000380070.1:p.Lys3Met
ENST00000466525.1:n.49A>T
ENST00000466588.5:n.87A>T
ENST00000474249.5:n.60A>T
ENST00000492719.5:n.68A>T
ENST00000496049.1:n.89A>T
NM_001289745.1:c.8A>T	NP_001276674.1:p.Lys3Met
NM_001289746.1:c.8A>T	NP_001276675.1:p.Lys3Met
NM_002046.5:c.8A>T	NP_002037.2:p.Lys3Met
NM_001289745.2:c.8A>T	NP_001276674.1:p.Lys3Met
NM_001357943.1:c.8A>T	NP_001344872.1:p.Lys3Met
NM_002046.6:c.8A>T	NP_002037.2:p.Lys3Met
NR_152150.1:n.84A>T
NM_002046.7:c.8A>T MANE Select	NP_002037.2:p.Lys3Met
NM_001289745.3:c.8A>T	NP_001276674.1:p.Lys3Met
NM_001289746.2:c.8A>T	NP_001276675.1:p.Lys3Met
NM_001357943.2:c.8A>T	NP_001344872.1:p.Lys3Met
NR_152150.2:n.84A>T