Canonical Allele Identifier: CA1172961723
Gene: SLC35D1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009364C= , CM000663.2:g.67009364C= GRCh38
NC_000001.10:g.67475047C= , CM000663.1:g.67475047C= GRCh37
NC_000001.9:g.67247635C= NCBI36
NG_012933.1:g.50034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-197G= MANE Select ENSP00000235345.5:n.877-197G=
ENST00000235345.5:c.877-197G= ENSP00000235345.5:n.877-197G=
NM_015139.2:c.877-197G= NP_055954.1:n.877-197G=
XM_006710478.1:c.958-197G= XP_006710541.1:n.958-197G=
XM_011541070.1:c.958-197G= XP_011539372.1:n.958-197G=
XM_006710478.2:c.958-197G= XP_006710541.1:n.958-197G=
XM_011541070.2:c.958-197G= XP_011539372.1:n.958-197G=
XR_001737057.2:n.1461-197G=
XR_001737058.2:n.2246-197G=
NM_015139.3:c.877-197G= MANE Select NP_055954.1:n.877-197G=