Canonical Allele Identifier: CA339960884
Gene: SLC2A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930746G>C , CM000663.2:g.42930746G>C GRCh38
NC_000001.10:g.43396417G>C , CM000663.1:g.43396417G>C GRCh37
NC_000001.9:g.43169004G>C NCBI36
NG_008232.1:g.33431C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.396C>G MANE Select ENSP00000416293.2:p.Tyr132Ter
ENST00000674765.1:c.396C>G ENSP00000501811.1:p.Tyr132Ter
ENST00000675112.1:n.419C>G
ENST00000676254.1:n.845C>G
ENST00000372500.4:c.300C>G ENSP00000361578.4:p.Tyr100Ter
ENST00000426263.7:c.396C>G ENSP00000416293.2:p.Tyr132Ter
ENST00000439722.2:c.275C>G ENSP00000395521.2:n.275C>G
ENST00000475162.3:c.295C>G
ENST00000625233.2:n.604C>G
ENST00000630287.2:c.396C>G ENSP00000486694.1:p.Tyr132Ter
NM_006516.2:c.396C>G NP_006507.2:p.Tyr132Ter
NM_006516.3:c.396C>G NP_006507.2:p.Tyr132Ter
NM_006516.4:c.396C>G MANE Select NP_006507.2:p.Tyr132Ter