Canonical Allele Identifier: CA340708578
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053894A>T , CM000663.2:g.67053894A>T GRCh38
NC_000001.10:g.67519577A>T , CM000663.1:g.67519577A>T GRCh37
NC_000001.9:g.67292165A>T NCBI36
NG_012933.1:g.5504T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.120T>A MANE Select ENSP00000235345.5:p.Phe40Leu
ENST00000235345.5:c.120T>A ENSP00000235345.5:p.Phe40Leu
NM_015139.2:c.120T>A NP_055954.1:p.Phe40Leu
XM_006710478.1:c.120T>A XP_006710541.1:p.Phe40Leu
XM_011541070.1:c.120T>A XP_011539372.1:p.Phe40Leu
XM_006710478.2:c.120T>A XP_006710541.1:p.Phe40Leu
XM_011541070.2:c.120T>A XP_011539372.1:p.Phe40Leu
XR_001737057.2:n.530T>A
XR_001737058.2:n.523T>A
NM_015139.3:c.120T>A MANE Select NP_055954.1:p.Phe40Leu