Canonical Allele Identifier: CA1172975844
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054004C= , CM000663.2:g.67054004C= GRCh38
NC_000001.10:g.67519687C= , CM000663.1:g.67519687C= GRCh37
NC_000001.9:g.67292275C= NCBI36
NG_012933.1:g.5394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.10G= MANE Select ENSP00000235345.5:p.Val4=
ENST00000235345.5:c.10G= ENSP00000235345.5:p.Val4=
NM_015139.2:c.10G= NP_055954.1:p.Val4=
XM_006710478.1:c.10G= XP_006710541.1:p.Val4=
XM_011541070.1:c.10G= XP_011539372.1:p.Val4=
XM_006710478.2:c.10G= XP_006710541.1:p.Val4=
XM_011541070.2:c.10G= XP_011539372.1:p.Val4=
XR_001737057.2:n.420G=
XR_001737058.2:n.413G=
NM_015139.3:c.10G= MANE Select NP_055954.1:p.Val4=