Canonical Allele Identifier: CA1002734986
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1570607375
gnomAD v3: 1-67009019-C-A
gnomAD v4: 1-67009019-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009019C>A , CM000663.2:g.67009019C>A GRCh38
NC_000001.10:g.67474702C>A , CM000663.1:g.67474702C>A GRCh37
NC_000001.9:g.67247290C>A NCBI36
NG_012933.1:g.50379G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.959+66G>T MANE Select ENSP00000235345.5:n.959+66G>T
ENST00000235345.5:c.959+66G>T ENSP00000235345.5:n.959+66G>T
NM_015139.2:c.959+66G>T NP_055954.1:n.959+66G>T
XM_006710478.1:c.1040+66G>T XP_006710541.1:n.1040+66G>T
XM_011541070.1:c.1040+66G>T XP_011539372.1:n.1040+66G>T
XM_006710478.2:c.1040+66G>T XP_006710541.1:n.1040+66G>T
XM_011541070.2:c.1040+66G>T XP_011539372.1:n.1040+66G>T
XR_001737057.2:n.1543+66G>T
XR_001737058.2:n.2328+66G>T
NM_015139.3:c.959+66G>T MANE Select NP_055954.1:n.959+66G>T