Canonical Allele Identifier: CA944359723

Gene: GAPDH

Linked Data

• dbSNP Id: rs1946418099
• gnomAD v3: 12-6534681-G-GC
• gnomAD v4: 12-6534681-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534682dup , CM000674.2:g.6534682dup	GRCh38
NC_000012.11:g.6643848dup , CM000674.1:g.6643848dup	GRCh37
NC_000012.10:g.6514109dup	NCBI36
NG_007073.2:g.5192dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+113dup MANE Select	ENSP00000229239.5:n.-24+113dup
ENST00000229239.9:c.-24+113dup	ENSP00000229239.5:n.-24+113dup
ENST00000396856.5:c.-276+113dup	ENSP00000380065.1:n.-276+113dup
ENST00000396861.5:c.-24+21dup	ENSP00000380070.1:n.-24+21dup
ENST00000474249.5:n.29+113dup
ENST00000492719.5:n.37+113dup
ENST00000496049.1:n.58+113dup
NM_001289745.1:c.-24+21dup	NP_001276674.1:n.-24+21dup
NM_001289746.1:c.-151dup	NP_001276675.1:n.-151dup
NM_002046.5:c.-24+113dup	NP_002037.2:n.-24+113dup
NM_001289745.2:c.-24+21dup	NP_001276674.1:n.-24+21dup
NM_001357943.1:c.-24+113dup	NP_001344872.1:n.-24+113dup
NM_002046.6:c.-24+113dup	NP_002037.2:n.-24+113dup
NR_152150.1:n.53+113dup
NM_002046.7:c.-24+113dup MANE Select	NP_002037.2:n.-24+113dup
NM_001289745.3:c.-24+21dup	NP_001276674.1:n.-24+21dup
NM_001289746.2:c.-151dup	NP_001276675.1:n.-151dup
NM_001357943.2:c.-24+113dup	NP_001344872.1:n.-24+113dup
NR_152150.2:n.53+113dup