Canonical Allele Identifier: CA436772993

Gene: SLC2A2

Linked Data

• MyVariant Identifiers: chr3:g.170716099G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.170998310G>C , CM000665.2:g.170998310G>C	GRCh38
NC_000003.11:g.170716099G>C , CM000665.1:g.170716099G>C	GRCh37
NC_000003.10:g.172198793G>C	NCBI36
NG_008108.1:g.33670C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000314251.8:c.1257C>G MANE Select	ENSP00000323568.3:p.Pro419=
ENST00000314251.7:c.1257C>G	ENSP00000323568.3:p.Pro419=
ENST00000469787.1:c.*724C>G	ENSP00000417918.1:n.*724C>G
ENST00000497642.5:c.*724C>G	ENSP00000418456.1:n.*724C>G
NM_000340.1:c.1257C>G	NP_000331.1:p.Pro419=
NM_001278658.1:c.900C>G	NP_001265587.1:p.Pro300=
NM_001278659.1:c.738C>G	NP_001265588.1:p.Pro246=
XM_011513087.1:c.1212C>G	XP_011511389.1:p.Pro404=
XM_011513088.1:c.1038C>G	XP_011511390.1:p.Pro346=
XM_011513089.1:c.738C>G	XP_011511391.1:p.Pro246=
XM_011513087.2:c.1212C>G	XP_011511389.1:p.Pro404=
XM_024453720.1:c.738C>G	XP_024309488.1:p.Pro246=
NM_000340.2:c.1257C>G MANE Select	NP_000331.1:p.Pro419=
NM_001278658.2:c.900C>G	NP_001265587.1:p.Pro300=
NM_001278659.2:c.738C>G	NP_001265588.1:p.Pro246=