Canonical Allele Identifier: CA1165411598
Gene: SLC2A1 HGNC NCBI

Linked Data

dbSNP Id: rs1643444535

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927856G>A , CM000663.2:g.42927856G>A GRCh38
NC_000001.10:g.43393527G>A , CM000663.1:g.43393527G>A GRCh37
NC_000001.9:g.43166114G>A NCBI36
NG_008232.1:g.36321C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1075-48C>T MANE Select ENSP00000416293.2:n.1075-48C>T
ENST00000674545.1:n.1644C>T
ENST00000674765.1:c.1030-999C>T ENSP00000501811.1:n.1030-999C>T
ENST00000675112.1:n.1376-48C>T
ENST00000676254.1:n.1524-48C>T
ENST00000426263.7:c.1075-48C>T ENSP00000416293.2:n.1075-48C>T
ENST00000475162.3:c.416-878C>T
ENST00000630287.2:c.*390-48C>T ENSP00000486694.1:n.*390-48C>T
NM_006516.2:c.1075-48C>T NP_006507.2:n.1075-48C>T
NM_006516.3:c.1075-48C>T NP_006507.2:n.1075-48C>T
NM_006516.4:c.1075-48C>T MANE Select NP_006507.2:n.1075-48C>T