Canonical Allele Identifier: CA1172975991
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054099G= , CM000663.2:g.67054099G= GRCh38
NC_000001.10:g.67519782G= , CM000663.1:g.67519782G= GRCh37
NC_000001.9:g.67292370G= NCBI36
NG_012933.1:g.5299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-86C= MANE Select ENSP00000235345.5:n.-86C=
ENST00000235345.5:c.-86C= ENSP00000235345.5:n.-86C=
NM_015139.2:c.-86C= NP_055954.1:n.-86C=
XM_006710478.1:c.-86C= XP_006710541.1:n.-86C=
XM_011541070.1:c.-86C= XP_011539372.1:n.-86C=
XM_006710478.2:c.-86C= XP_006710541.1:n.-86C=
XM_011541070.2:c.-86C= XP_011539372.1:n.-86C=
XR_001737057.2:n.325C=
XR_001737058.2:n.318C=
NM_015139.3:c.-86C= MANE Select NP_055954.1:n.-86C=