Canonical Allele Identifier: CA2645198861
Gene: SLC2A1 HGNC NCBI

Linked Data

gnomAD v4: 1-42929037-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42929037T>G , CM000663.2:g.42929037T>G GRCh38
NC_000001.10:g.43394708T>G , CM000663.1:g.43394708T>G GRCh37
NC_000001.9:g.43167295T>G NCBI36
NG_008232.1:g.35140A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000426263.10:c.973-4A>C MANE Select ENSP00000416293.2:n.973-4A>C
ENST00000674545.1:n.463A>C
ENST00000674765.1:c.973-4A>C ENSP00000501811.1:n.973-4A>C
ENST00000675112.1:n.1274-4A>C
ENST00000676254.1:n.1422-4A>C
ENST00000426263.7:c.973-4A>C ENSP00000416293.2:n.973-4A>C
ENST00000439722.2:c.852-4A>C ENSP00000395521.2:n.852-4A>C
ENST00000475162.3:c.415+1589A>C
ENST00000630287.2:c.*288-4A>C ENSP00000486694.1:n.*288-4A>C
NM_006516.2:c.973-4A>C NP_006507.2:n.973-4A>C
NM_006516.3:c.973-4A>C NP_006507.2:n.973-4A>C
NM_006516.4:c.973-4A>C MANE Select NP_006507.2:n.973-4A>C