Canonical Allele Identifier: CA1172976006
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645347110
gnomAD v4: 1-67054108-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054108G>A , CM000663.2:g.67054108G>A GRCh38
NC_000001.10:g.67519791G>A , CM000663.1:g.67519791G>A GRCh37
NC_000001.9:g.67292379G>A NCBI36
NG_012933.1:g.5290C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-95C>T MANE Select ENSP00000235345.5:n.-95C>T
NM_015139.2:c.-95C>T NP_055954.1:n.-95C>T
XM_006710478.1:c.-95C>T XP_006710541.1:n.-95C>T
XM_011541070.1:c.-95C>T XP_011539372.1:n.-95C>T
XM_006710478.2:c.-95C>T XP_006710541.1:n.-95C>T
XM_011541070.2:c.-95C>T XP_011539372.1:n.-95C>T
XR_001737057.2:n.316C>T
XR_001737058.2:n.309C>T
NM_015139.3:c.-95C>T MANE Select NP_055954.1:n.-95C>T