Canonical Allele Identifier: CA2696040786
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs2102385272

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054081A>C , CM000663.2:g.67054081A>C GRCh38
NC_000001.10:g.67519764A>C , CM000663.1:g.67519764A>C GRCh37
NC_000001.9:g.67292352A>C NCBI36
NG_012933.1:g.5317T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-68T>G MANE Select ENSP00000235345.5:n.-68T>G
ENST00000235345.5:c.-68T>G ENSP00000235345.5:n.-68T>G
NM_015139.2:c.-68T>G NP_055954.1:n.-68T>G
XM_006710478.1:c.-68T>G XP_006710541.1:n.-68T>G
XM_011541070.1:c.-68T>G XP_011539372.1:n.-68T>G
XM_006710478.2:c.-68T>G XP_006710541.1:n.-68T>G
XM_011541070.2:c.-68T>G XP_011539372.1:n.-68T>G
XR_001737057.2:n.343T>G
XR_001737058.2:n.336T>G
NM_015139.3:c.-68T>G MANE Select NP_055954.1:n.-68T>G