Canonical Allele Identifier: CA417406701

Gene: SLC2A1

Linked Data

• MyVariant Identifiers: chr1:g.43393321G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42927650G>A , CM000663.2:g.42927650G>A	GRCh38
NC_000001.10:g.43393321G>A , CM000663.1:g.43393321G>A	GRCh37
NC_000001.9:g.43165908G>A	NCBI36
NG_008232.1:g.36527C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426263.10:c.1233C>T MANE Select	ENSP00000416293.2:p.Asn411=
ENST00000674545.1:n.1850C>T
ENST00000674765.1:c.1030-793C>T	ENSP00000501811.1:n.1030-793C>T
ENST00000675112.1:n.1534C>T
ENST00000676254.1:n.1682C>T
ENST00000426263.7:c.1233C>T	ENSP00000416293.2:p.Asn411=
ENST00000475162.3:c.416-672C>T
ENST00000630287.2:c.*548C>T	ENSP00000486694.1:n.*548C>T
NM_006516.2:c.1233C>T	NP_006507.2:p.Asn411=
NM_006516.3:c.1233C>T	NP_006507.2:p.Asn411=
NM_006516.4:c.1233C>T MANE Select	NP_006507.2:p.Asn411=