Canonical Allele Identifier: CA2645199502
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42930137-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930137G>T , CM000663.2:g.42930137G>T GRCh38
NC_000001.10:g.43395808G>T , CM000663.1:g.43395808G>T GRCh37
NC_000001.9:g.43168395G>T NCBI36
NG_008232.1:g.34040C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-102C>A MANE Select ENSP00000416293.2:n.517-102C>A
ENST00000674765.1:c.517-102C>A ENSP00000501811.1:n.517-102C>A
ENST00000675112.1:n.540-102C>A
ENST00000676254.1:n.966-102C>A
ENST00000426263.7:c.517-102C>A ENSP00000416293.2:n.517-102C>A
ENST00000439722.2:c.396-102C>A ENSP00000395521.2:n.396-102C>A
ENST00000475162.3:c.415+489C>A
ENST00000630287.2:c.517-357C>A ENSP00000486694.1:n.517-357C>A
NM_006516.2:c.517-102C>A NP_006507.2:n.517-102C>A
NM_006516.3:c.517-102C>A NP_006507.2:n.517-102C>A
NM_006516.4:c.517-102C>A MANE Select NP_006507.2:n.517-102C>A