Canonical Allele Identifier: CA24005534
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs925450718
gnomAD v4: 1-67009125-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67009125A>G , CM000663.2:g.67009125A>G GRCh38
NC_000001.10:g.67474808A>G , CM000663.1:g.67474808A>G GRCh37
NC_000001.9:g.67247396A>G NCBI36
NG_012933.1:g.50273T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.919T>C MANE Select ENSP00000235345.5:p.Tyr307His
ENST00000235345.5:c.919T>C ENSP00000235345.5:p.Tyr307His
NM_015139.2:c.919T>C NP_055954.1:p.Tyr307His
XM_006710478.1:c.1000T>C XP_006710541.1:p.Tyr334His
XM_011541070.1:c.1000T>C XP_011539372.1:p.Tyr334His
XM_006710478.2:c.1000T>C XP_006710541.1:p.Tyr334His
XM_011541070.2:c.1000T>C XP_011539372.1:p.Tyr334His
XR_001737057.2:n.1503T>C
XR_001737058.2:n.2288T>C
NM_015139.3:c.919T>C MANE Select NP_055954.1:p.Tyr307His