Canonical Allele Identifier: CA355490410

Gene: SLC2A2

Linked Data

• MyVariant Identifiers: chr3:g.170724962A>C (hg19) ; chr3:g.171007173A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007173A>C , CM000665.2:g.171007173A>C	GRCh38
NC_000003.11:g.170724962A>C , CM000665.1:g.170724962A>C	GRCh37
NC_000003.10:g.172207656A>C	NCBI36
NG_008108.1:g.24807T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.587T>G MANE Select	ENSP00000323568.3:p.Ile196Ser
ENST00000314251.7:c.587T>G	ENSP00000323568.3:p.Ile196Ser
ENST00000461867.1:c.68T>G	ENSP00000418888.1:p.Ile23Ser
ENST00000469787.1:c.*54T>G	ENSP00000417918.1:n.*54T>G
ENST00000471379.1:n.298T>G
ENST00000497642.5:c.*54T>G	ENSP00000418456.1:n.*54T>G
NM_000340.1:c.587T>G	NP_000331.1:p.Ile196Ser
NM_001278658.1:c.230T>G	NP_001265587.1:p.Ile77Ser
NM_001278659.1:c.68T>G	NP_001265588.1:p.Ile23Ser
XM_011513087.1:c.542T>G	XP_011511389.1:p.Ile181Ser
XM_011513088.1:c.368T>G	XP_011511390.1:p.Ile123Ser
XM_011513089.1:c.68T>G	XP_011511391.1:p.Ile23Ser
XM_011513087.2:c.542T>G	XP_011511389.1:p.Ile181Ser
XM_024453720.1:c.68T>G	XP_024309488.1:p.Ile23Ser
NM_000340.2:c.587T>G MANE Select	NP_000331.1:p.Ile196Ser
NM_001278658.2:c.230T>G	NP_001265587.1:p.Ile77Ser
NM_001278659.2:c.68T>G	NP_001265588.1:p.Ile23Ser