Canonical Allele Identifier: CA1165411502

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927592T= , CM000663.2:g.42927592T=	GRCh38
NC_000001.10:g.43393263T= , CM000663.1:g.43393263T=	GRCh37
NC_000001.9:g.43165850T=	NCBI36
NG_008232.1:g.36585A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1278+13A= MANE Select	ENSP00000416293.2:n.1278+13A=
ENST00000674545.1:n.1895+13A=
ENST00000674765.1:c.1030-735A=	ENSP00000501811.1:n.1030-735A=
ENST00000675112.1:n.1579+13A=
ENST00000676254.1:n.1727+13A=
ENST00000426263.7:c.1278+13A=	ENSP00000416293.2:n.1278+13A=
ENST00000475162.3:c.416-614A=
ENST00000630287.2:c.*593+13A=	ENSP00000486694.1:n.*593+13A=
NM_006516.2:c.1278+13A=	NP_006507.2:n.1278+13A=
NM_006516.3:c.1278+13A=	NP_006507.2:n.1278+13A=
NM_006516.4:c.1278+13A= MANE Select	NP_006507.2:n.1278+13A=