Canonical Allele Identifier: CA899217
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs760859292
gnomAD v2: 1-67519720-G-A
gnomAD v4: 1-67054037-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054037G>A , CM000663.2:g.67054037G>A GRCh38
NC_000001.10:g.67519720G>A , CM000663.1:g.67519720G>A GRCh37
NC_000001.9:g.67292308G>A NCBI36
NG_012933.1:g.5361C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-24C>T MANE Select ENSP00000235345.5:n.-24C>T
ENST00000235345.5:c.-24C>T ENSP00000235345.5:n.-24C>T
NM_015139.2:c.-24C>T NP_055954.1:n.-24C>T
XM_006710478.1:c.-24C>T XP_006710541.1:n.-24C>T
XM_011541070.1:c.-24C>T XP_011539372.1:n.-24C>T
XM_006710478.2:c.-24C>T XP_006710541.1:n.-24C>T
XM_011541070.2:c.-24C>T XP_011539372.1:n.-24C>T
XR_001737057.2:n.387C>T
XR_001737058.2:n.380C>T
NM_015139.3:c.-24C>T MANE Select NP_055954.1:n.-24C>T