Canonical Allele Identifier: CA1172975896
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645345769

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054040G>A , CM000663.2:g.67054040G>A GRCh38
NC_000001.10:g.67519723G>A , CM000663.1:g.67519723G>A GRCh37
NC_000001.9:g.67292311G>A NCBI36
NG_012933.1:g.5358C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-27C>T MANE Select ENSP00000235345.5:n.-27C>T
ENST00000235345.5:c.-27C>T ENSP00000235345.5:n.-27C>T
NM_015139.2:c.-27C>T NP_055954.1:n.-27C>T
XM_006710478.1:c.-27C>T XP_006710541.1:n.-27C>T
XM_011541070.1:c.-27C>T XP_011539372.1:n.-27C>T
XM_006710478.2:c.-27C>T XP_006710541.1:n.-27C>T
XM_011541070.2:c.-27C>T XP_011539372.1:n.-27C>T
XR_001737057.2:n.384C>T
XR_001737058.2:n.377C>T
NM_015139.3:c.-27C>T MANE Select NP_055954.1:n.-27C>T