Canonical Allele Identifier: CA232400018

Gene: GAPDH

Linked Data

• dbSNP Id: rs575095159
• gnomAD v2: 12-6643906-G-T
• gnomAD v3: 12-6534740-G-T
• gnomAD v4: 12-6534740-G-T
• MyVariant Identifiers: chr12:g.6643906G>T (hg19) ; chr12:g.6534740G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534740G>T , CM000674.2:g.6534740G>T	GRCh38
NC_000012.11:g.6643906G>T , CM000674.1:g.6643906G>T	GRCh37
NC_000012.10:g.6514167G>T	NCBI36
NG_007073.2:g.5250G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-23-70G>T MANE Select	ENSP00000229239.5:n.-23-70G>T
ENST00000229239.9:c.-23-70G>T	ENSP00000229239.5:n.-23-70G>T
ENST00000396856.5:c.-275-70G>T	ENSP00000380065.1:n.-275-70G>T
ENST00000396861.5:c.-23-70G>T	ENSP00000380070.1:n.-23-70G>T
ENST00000474249.5:n.30-70G>T
ENST00000492719.5:n.38-70G>T
ENST00000496049.1:n.59-70G>T
NM_001289745.1:c.-23-70G>T	NP_001276674.1:n.-23-70G>T
NM_001289746.1:c.-93G>T	NP_001276675.1:n.-93G>T
NM_002046.5:c.-23-70G>T	NP_002037.2:n.-23-70G>T
NM_001289745.2:c.-23-70G>T	NP_001276674.1:n.-23-70G>T
NM_001357943.1:c.-23-70G>T	NP_001344872.1:n.-23-70G>T
NM_002046.6:c.-23-70G>T	NP_002037.2:n.-23-70G>T
NR_152150.1:n.54-70G>T
NM_002046.7:c.-23-70G>T MANE Select	NP_002037.2:n.-23-70G>T
NM_001289745.3:c.-23-70G>T	NP_001276674.1:n.-23-70G>T
NM_001289746.2:c.-93G>T	NP_001276675.1:n.-93G>T
NM_001357943.2:c.-23-70G>T	NP_001344872.1:n.-23-70G>T
NR_152150.2:n.54-70G>T