Canonical Allele Identifier: CA2668525086

Gene: SLC2A2

Linked Data

• gnomAD v4: 3-171007026-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007026A>C , CM000665.2:g.171007026A>C	GRCh38
NC_000003.11:g.170724815A>C , CM000665.1:g.170724815A>C	GRCh37
NC_000003.10:g.172207509A>C	NCBI36
NG_008108.1:g.24954T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.612+122T>G MANE Select	ENSP00000323568.3:n.612+122T>G
ENST00000314251.7:c.612+122T>G	ENSP00000323568.3:n.612+122T>G
ENST00000461867.1:c.93+122T>G	ENSP00000418888.1:n.93+122T>G
ENST00000469787.1:c.*79+122T>G	ENSP00000417918.1:n.*79+122T>G
ENST00000471379.1:n.323+122T>G
ENST00000497642.5:c.*79+122T>G	ENSP00000418456.1:n.*79+122T>G
NM_000340.1:c.612+122T>G	NP_000331.1:n.612+122T>G
NM_001278658.1:c.255+122T>G	NP_001265587.1:n.255+122T>G
NM_001278659.1:c.93+122T>G	NP_001265588.1:n.93+122T>G
XM_011513087.1:c.567+122T>G	XP_011511389.1:n.567+122T>G
XM_011513088.1:c.393+122T>G	XP_011511390.1:n.393+122T>G
XM_011513089.1:c.93+122T>G	XP_011511391.1:n.93+122T>G
XM_011513087.2:c.567+122T>G	XP_011511389.1:n.567+122T>G
XM_024453720.1:c.93+122T>G	XP_024309488.1:n.93+122T>G
NM_000340.2:c.612+122T>G MANE Select	NP_000331.1:n.612+122T>G
NM_001278658.2:c.255+122T>G	NP_001265587.1:n.255+122T>G
NM_001278659.2:c.93+122T>G	NP_001265588.1:n.93+122T>G