Canonical Allele Identifier: CA340708692
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053953A>T , CM000663.2:g.67053953A>T GRCh38
NC_000001.10:g.67519636A>T , CM000663.1:g.67519636A>T GRCh37
NC_000001.9:g.67292224A>T NCBI36
NG_012933.1:g.5445T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.61T>A MANE Select ENSP00000235345.5:p.Ser21Thr
ENST00000235345.5:c.61T>A ENSP00000235345.5:p.Ser21Thr
NM_015139.2:c.61T>A NP_055954.1:p.Ser21Thr
XM_006710478.1:c.61T>A XP_006710541.1:p.Ser21Thr
XM_011541070.1:c.61T>A XP_011539372.1:p.Ser21Thr
XM_006710478.2:c.61T>A XP_006710541.1:p.Ser21Thr
XM_011541070.2:c.61T>A XP_011539372.1:p.Ser21Thr
XR_001737057.2:n.471T>A
XR_001737058.2:n.464T>A
NM_015139.3:c.61T>A MANE Select NP_055954.1:p.Ser21Thr