Canonical Allele Identifier: CA2646117949
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67054039-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054039C>G , CM000663.2:g.67054039C>G GRCh38
NC_000001.10:g.67519722C>G , CM000663.1:g.67519722C>G GRCh37
NC_000001.9:g.67292310C>G NCBI36
NG_012933.1:g.5359G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-26G>C MANE Select ENSP00000235345.5:n.-26G>C
ENST00000235345.5:c.-26G>C ENSP00000235345.5:n.-26G>C
NM_015139.2:c.-26G>C NP_055954.1:n.-26G>C
XM_006710478.1:c.-26G>C XP_006710541.1:n.-26G>C
XM_011541070.1:c.-26G>C XP_011539372.1:n.-26G>C
XM_006710478.2:c.-26G>C XP_006710541.1:n.-26G>C
XM_011541070.2:c.-26G>C XP_011539372.1:n.-26G>C
XR_001737057.2:n.385G>C
XR_001737058.2:n.378G>C
NM_015139.3:c.-26G>C MANE Select NP_055954.1:n.-26G>C