Canonical Allele Identifier: CA340708762
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67053989-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053989G>A , CM000663.2:g.67053989G>A GRCh38
NC_000001.10:g.67519672G>A , CM000663.1:g.67519672G>A GRCh37
NC_000001.9:g.67292260G>A NCBI36
NG_012933.1:g.5409C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.25C>T MANE Select ENSP00000235345.5:p.His9Tyr
ENST00000235345.5:c.25C>T ENSP00000235345.5:p.His9Tyr
NM_015139.2:c.25C>T NP_055954.1:p.His9Tyr
XM_006710478.1:c.25C>T XP_006710541.1:p.His9Tyr
XM_011541070.1:c.25C>T XP_011539372.1:p.His9Tyr
XM_006710478.2:c.25C>T XP_006710541.1:p.His9Tyr
XM_011541070.2:c.25C>T XP_011539372.1:p.His9Tyr
XR_001737057.2:n.435C>T
XR_001737058.2:n.428C>T
NM_015139.3:c.25C>T MANE Select NP_055954.1:p.His9Tyr