Canonical Allele Identifier: CA1172975817
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053975T= , CM000663.2:g.67053975T= GRCh38
NC_000001.10:g.67519658T= , CM000663.1:g.67519658T= GRCh37
NC_000001.9:g.67292246T= NCBI36
NG_012933.1:g.5423A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.39A= MANE Select ENSP00000235345.5:p.Lys13=
ENST00000235345.5:c.39A= ENSP00000235345.5:p.Lys13=
NM_015139.2:c.39A= NP_055954.1:p.Lys13=
XM_006710478.1:c.39A= XP_006710541.1:p.Lys13=
XM_011541070.1:c.39A= XP_011539372.1:p.Lys13=
XM_006710478.2:c.39A= XP_006710541.1:p.Lys13=
XM_011541070.2:c.39A= XP_011539372.1:p.Lys13=
XR_001737057.2:n.449A=
XR_001737058.2:n.442A=
NM_015139.3:c.39A= MANE Select NP_055954.1:p.Lys13=