Canonical Allele Identifier: CA355490462

Gene: SLC2A2

Linked Data

• MyVariant Identifiers: chr3:g.170724974T>A (hg19) ; chr3:g.171007185T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.171007185T>A , CM000665.2:g.171007185T>A	GRCh38
NC_000003.11:g.170724974T>A , CM000665.1:g.170724974T>A	GRCh37
NC_000003.10:g.172207668T>A	NCBI36
NG_008108.1:g.24795A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314251.8:c.575A>T MANE Select	ENSP00000323568.3:p.His192Leu
ENST00000314251.7:c.575A>T	ENSP00000323568.3:p.His192Leu
ENST00000461867.1:c.56A>T	ENSP00000418888.1:p.His19Leu
ENST00000469787.1:c.*42A>T	ENSP00000417918.1:n.*42A>T
ENST00000471379.1:n.286A>T
ENST00000497642.5:c.*42A>T	ENSP00000418456.1:n.*42A>T
NM_000340.1:c.575A>T	NP_000331.1:p.His192Leu
NM_001278658.1:c.218A>T	NP_001265587.1:p.His73Leu
NM_001278659.1:c.56A>T	NP_001265588.1:p.His19Leu
XM_011513087.1:c.530A>T	XP_011511389.1:p.His177Leu
XM_011513088.1:c.356A>T	XP_011511390.1:p.His119Leu
XM_011513089.1:c.56A>T	XP_011511391.1:p.His19Leu
XM_011513087.2:c.530A>T	XP_011511389.1:p.His177Leu
XM_024453720.1:c.56A>T	XP_024309488.1:p.His19Leu
NM_000340.2:c.575A>T MANE Select	NP_000331.1:p.His192Leu
NM_001278658.2:c.218A>T	NP_001265587.1:p.His73Leu
NM_001278659.2:c.56A>T	NP_001265588.1:p.His19Leu