Canonical Allele Identifier: CA1165412377
Gene: SLC2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929726T= , CM000663.2:g.42929726T= GRCh38
NC_000001.10:g.43395397T= , CM000663.1:g.43395397T= GRCh37
NC_000001.9:g.43167984T= NCBI36
NG_008232.1:g.34451A=

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.734A= MANE Select ENSP00000416293.2:p.Lys245=
ENST00000669445.1:c.64A=
ENST00000674765.1:c.734A= ENSP00000501811.1:p.Lys245=
ENST00000675112.1:n.757A=
ENST00000676254.1:n.1183A=
ENST00000426263.7:c.734A= ENSP00000416293.2:p.Lys245=
ENST00000439722.2:c.613A= ENSP00000395521.2:n.613A=
ENST00000475162.3:c.415+900A=
ENST00000630287.2:c.*49A= ENSP00000486694.1:n.*49A=
NM_006516.2:c.734A= NP_006507.2:p.Lys245=
NM_006516.3:c.734A= NP_006507.2:p.Lys245=
NM_006516.4:c.734A= MANE Select NP_006507.2:p.Lys245=