Canonical Allele Identifier: CA2617278571

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534622-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534626dup , CM000674.2:g.6534626dup	GRCh38
NC_000012.11:g.6643792dup , CM000674.1:g.6643792dup	GRCh37
NC_000012.10:g.6514053dup	NCBI36
NG_007073.2:g.5136dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-24+57dup MANE Select	ENSP00000229239.5:n.-24+57dup
ENST00000229239.9:c.-24+57dup	ENSP00000229239.5:n.-24+57dup
ENST00000396856.5:c.-276+57dup	ENSP00000380065.1:n.-276+57dup
ENST00000396861.5:c.-59dup	ENSP00000380070.1:n.-59dup
ENST00000474249.5:n.29+57dup
ENST00000492719.5:n.37+57dup
ENST00000496049.1:n.58+57dup
NM_001289745.1:c.-59dup	NP_001276674.1:n.-59dup
NM_002046.5:c.-24+57dup	NP_002037.2:n.-24+57dup
NM_001289745.2:c.-59dup	NP_001276674.1:n.-59dup
NM_001357943.1:c.-24+57dup	NP_001344872.1:n.-24+57dup
NM_002046.6:c.-24+57dup	NP_002037.2:n.-24+57dup
NR_152150.1:n.53+57dup
NM_002046.7:c.-24+57dup MANE Select	NP_002037.2:n.-24+57dup
NM_001289745.3:c.-59dup	NP_001276674.1:n.-59dup
NM_001289746.2:c.-207dup	NP_001276675.1:n.-207dup
NM_001357943.2:c.-24+57dup	NP_001344872.1:n.-24+57dup
NR_152150.2:n.53+57dup