Canonical Allele Identifier: CA1165411508
Gene: SLC2A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42927602C= , CM000663.2:g.42927602C= GRCh38
NC_000001.10:g.43393273C= , CM000663.1:g.43393273C= GRCh37
NC_000001.9:g.43165860C= NCBI36
NG_008232.1:g.36575G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.1278+3G= MANE Select ENSP00000416293.2:n.1278+3G=
ENST00000674545.1:n.1895+3G=
ENST00000674765.1:c.1030-745G= ENSP00000501811.1:n.1030-745G=
ENST00000675112.1:n.1579+3G=
ENST00000676254.1:n.1727+3G=
ENST00000426263.7:c.1278+3G= ENSP00000416293.2:n.1278+3G=
ENST00000475162.3:c.416-624G=
ENST00000630287.2:c.*593+3G= ENSP00000486694.1:n.*593+3G=
NM_006516.2:c.1278+3G= NP_006507.2:n.1278+3G=
NM_006516.3:c.1278+3G= NP_006507.2:n.1278+3G=
NM_006516.4:c.1278+3G= MANE Select NP_006507.2:n.1278+3G=
Search 100 bp 5'
Search 100 bp 3'