Canonical Allele Identifier: CA1144228776

Gene: SLC2A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42929918G= , CM000663.2:g.42929918G=	GRCh38
NC_000001.10:g.43395589G= , CM000663.1:g.43395589G=	GRCh37
NC_000001.9:g.43168176G=	NCBI36
NG_008232.1:g.34259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.634C= MANE Select	ENSP00000416293.2:p.Arg212=
ENST00000669445.1:c.11C=
ENST00000674765.1:c.634C=	ENSP00000501811.1:p.Arg212=
ENST00000675112.1:n.657C=
ENST00000676254.1:n.1083C=
ENST00000426263.7:c.634C=	ENSP00000416293.2:p.Arg212=
ENST00000439722.2:c.513C=	ENSP00000395521.2:n.513C=
ENST00000475162.3:c.415+708C=
ENST00000630287.2:c.517-138C=	ENSP00000486694.1:n.517-138C=
NM_006516.2:c.634C=	NP_006507.2:p.Arg212=
NM_006516.3:c.634C=	NP_006507.2:p.Arg212=
NM_006516.4:c.634C= MANE Select	NP_006507.2:p.Arg212=