Canonical Allele Identifier: CA1165412145

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929169C= , CM000663.2:g.42929169C=	GRCh38
NC_000001.10:g.43394840C= , CM000663.1:g.43394840C=	GRCh37
NC_000001.9:g.43167427C=	NCBI36
NG_008232.1:g.35008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.972+41G= MANE Select	ENSP00000416293.2:n.972+41G=
ENST00000674545.1:n.331G=
ENST00000674765.1:c.972+41G=	ENSP00000501811.1:n.972+41G=
ENST00000675112.1:n.1273+41G=
ENST00000676254.1:n.1421+41G=
ENST00000426263.7:c.972+41G=	ENSP00000416293.2:n.972+41G=
ENST00000439722.2:c.851+41G=	ENSP00000395521.2:n.851+41G=
ENST00000475162.3:c.415+1457G=
ENST00000630287.2:c.*287+41G=	ENSP00000486694.1:n.*287+41G=
NM_006516.2:c.972+41G=	NP_006507.2:n.972+41G=
NM_006516.3:c.972+41G=	NP_006507.2:n.972+41G=
NM_006516.4:c.972+41G= MANE Select	NP_006507.2:n.972+41G=