Canonical Allele Identifier: CA2645199480
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42930121-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42930121C>A , CM000663.2:g.42930121C>A GRCh38
NC_000001.10:g.43395792C>A , CM000663.1:g.43395792C>A GRCh37
NC_000001.9:g.43168379C>A NCBI36
NG_008232.1:g.34056G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426263.10:c.517-86G>T MANE Select ENSP00000416293.2:n.517-86G>T
ENST00000674765.1:c.517-86G>T ENSP00000501811.1:n.517-86G>T
ENST00000675112.1:n.540-86G>T
ENST00000676254.1:n.966-86G>T
ENST00000426263.7:c.517-86G>T ENSP00000416293.2:n.517-86G>T
ENST00000439722.2:c.396-86G>T ENSP00000395521.2:n.396-86G>T
ENST00000475162.3:c.415+505G>T
ENST00000630287.2:c.517-341G>T ENSP00000486694.1:n.517-341G>T
NM_006516.2:c.517-86G>T NP_006507.2:n.517-86G>T
NM_006516.3:c.517-86G>T NP_006507.2:n.517-86G>T
NM_006516.4:c.517-86G>T MANE Select NP_006507.2:n.517-86G>T