Canonical Allele Identifier: CA355488301

Gene: SLC2A2

Linked Data

• MyVariant Identifiers: chr3:g.170723142T>C (hg19) ; chr3:g.171005353T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171005353T>C , CM000665.2:g.171005353T>C	GRCh38
NC_000003.11:g.170723142T>C , CM000665.1:g.170723142T>C	GRCh37
NC_000003.10:g.172205836T>C	NCBI36
NG_008108.1:g.26627A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.895A>G MANE Select	ENSP00000323568.3:p.Ser299Gly
ENST00000314251.7:c.895A>G	ENSP00000323568.3:p.Ser299Gly
ENST00000469787.1:c.*362A>G	ENSP00000417918.1:n.*362A>G
ENST00000497642.5:c.*362A>G	ENSP00000418456.1:n.*362A>G
NM_000340.1:c.895A>G	NP_000331.1:p.Ser299Gly
NM_001278658.1:c.538A>G	NP_001265587.1:p.Ser180Gly
NM_001278659.1:c.376A>G	NP_001265588.1:p.Ser126Gly
XM_011513087.1:c.850A>G	XP_011511389.1:p.Ser284Gly
XM_011513088.1:c.676A>G	XP_011511390.1:p.Ser226Gly
XM_011513089.1:c.376A>G	XP_011511391.1:p.Ser126Gly
XM_011513087.2:c.850A>G	XP_011511389.1:p.Ser284Gly
XM_024453720.1:c.376A>G	XP_024309488.1:p.Ser126Gly
NM_000340.2:c.895A>G MANE Select	NP_000331.1:p.Ser299Gly
NM_001278658.2:c.538A>G	NP_001265587.1:p.Ser180Gly
NM_001278659.2:c.376A>G	NP_001265588.1:p.Ser126Gly