Canonical Allele Identifier: CA1172975924
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054057C= , CM000663.2:g.67054057C= GRCh38
NC_000001.10:g.67519740C= , CM000663.1:g.67519740C= GRCh37
NC_000001.9:g.67292328C= NCBI36
NG_012933.1:g.5341G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-44G= MANE Select ENSP00000235345.5:n.-44G=
ENST00000235345.5:c.-44G= ENSP00000235345.5:n.-44G=
NM_015139.2:c.-44G= NP_055954.1:n.-44G=
XM_006710478.1:c.-44G= XP_006710541.1:n.-44G=
XM_011541070.1:c.-44G= XP_011539372.1:n.-44G=
XM_006710478.2:c.-44G= XP_006710541.1:n.-44G=
XM_011541070.2:c.-44G= XP_011539372.1:n.-44G=
XR_001737057.2:n.367G=
XR_001737058.2:n.360G=
NM_015139.3:c.-44G= MANE Select NP_055954.1:n.-44G=