Canonical Allele Identifier: CA1172961722
Gene: SLC35D1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009353C= , CM000663.2:g.67009353C= GRCh38
NC_000001.10:g.67475036C= , CM000663.1:g.67475036C= GRCh37
NC_000001.9:g.67247624C= NCBI36
NG_012933.1:g.50045G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.877-186G= MANE Select ENSP00000235345.5:n.877-186G=
ENST00000235345.5:c.877-186G= ENSP00000235345.5:n.877-186G=
NM_015139.2:c.877-186G= NP_055954.1:n.877-186G=
XM_006710478.1:c.958-186G= XP_006710541.1:n.958-186G=
XM_011541070.1:c.958-186G= XP_011539372.1:n.958-186G=
XM_006710478.2:c.958-186G= XP_006710541.1:n.958-186G=
XM_011541070.2:c.958-186G= XP_011539372.1:n.958-186G=
XR_001737057.2:n.1461-186G=
XR_001737058.2:n.2246-186G=
NM_015139.3:c.877-186G= MANE Select NP_055954.1:n.877-186G=
Search 100 bp 5'
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