Canonical Allele Identifier: CA2668525496

Gene: SLC2A2

Linked Data

• gnomAD v4: 3-171005269-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171005269G>C , CM000665.2:g.171005269G>C	GRCh38
NC_000003.11:g.170723058G>C , CM000665.1:g.170723058G>C	GRCh37
NC_000003.10:g.172205752G>C	NCBI36
NG_008108.1:g.26711C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.963+16C>G MANE Select	ENSP00000323568.3:n.963+16C>G
ENST00000314251.7:c.963+16C>G	ENSP00000323568.3:n.963+16C>G
ENST00000469787.1:c.*430+16C>G	ENSP00000417918.1:n.*430+16C>G
ENST00000497642.5:c.*430+16C>G	ENSP00000418456.1:n.*430+16C>G
NM_000340.1:c.963+16C>G	NP_000331.1:n.963+16C>G
NM_001278658.1:c.606+16C>G	NP_001265587.1:n.606+16C>G
NM_001278659.1:c.444+16C>G	NP_001265588.1:n.444+16C>G
XM_011513087.1:c.918+16C>G	XP_011511389.1:n.918+16C>G
XM_011513088.1:c.744+16C>G	XP_011511390.1:n.744+16C>G
XM_011513089.1:c.444+16C>G	XP_011511391.1:n.444+16C>G
XM_011513087.2:c.918+16C>G	XP_011511389.1:n.918+16C>G
XM_024453720.1:c.444+16C>G	XP_024309488.1:n.444+16C>G
NM_000340.2:c.963+16C>G MANE Select	NP_000331.1:n.963+16C>G
NM_001278658.2:c.606+16C>G	NP_001265587.1:n.606+16C>G
NM_001278659.2:c.444+16C>G	NP_001265588.1:n.444+16C>G