Canonical Allele Identifier: CA1172975969
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054085G= , CM000663.2:g.67054085G= GRCh38
NC_000001.10:g.67519768G= , CM000663.1:g.67519768G= GRCh37
NC_000001.9:g.67292356G= NCBI36
NG_012933.1:g.5313C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-72C= MANE Select ENSP00000235345.5:n.-72C=
ENST00000235345.5:c.-72C= ENSP00000235345.5:n.-72C=
NM_015139.2:c.-72C= NP_055954.1:n.-72C=
XM_006710478.1:c.-72C= XP_006710541.1:n.-72C=
XM_011541070.1:c.-72C= XP_011539372.1:n.-72C=
XM_006710478.2:c.-72C= XP_006710541.1:n.-72C=
XM_011541070.2:c.-72C= XP_011539372.1:n.-72C=
XR_001737057.2:n.339C=
XR_001737058.2:n.332C=
NM_015139.3:c.-72C= MANE Select NP_055954.1:n.-72C=