Canonical Allele Identifier: CA1172976019
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054121G= , CM000663.2:g.67054121G= GRCh38
NC_000001.10:g.67519804G= , CM000663.1:g.67519804G= GRCh37
NC_000001.9:g.67292392G= NCBI36
NG_012933.1:g.5277C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-108C= MANE Select ENSP00000235345.5:n.-108C=
NM_015139.2:c.-108C= NP_055954.1:n.-108C=
XM_006710478.1:c.-108C= XP_006710541.1:n.-108C=
XM_011541070.1:c.-108C= XP_011539372.1:n.-108C=
XM_006710478.2:c.-108C= XP_006710541.1:n.-108C=
XM_011541070.2:c.-108C= XP_011539372.1:n.-108C=
XR_001737057.2:n.303C=
XR_001737058.2:n.296C=
NM_015139.3:c.-108C= MANE Select NP_055954.1:n.-108C=