Canonical Allele Identifier: CA418437420
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67053969-T-C
MyVariant Identifiers: chr1:g.67519652T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053969T>C , CM000663.2:g.67053969T>C GRCh38
NC_000001.10:g.67519652T>C , CM000663.1:g.67519652T>C GRCh37
NC_000001.9:g.67292240T>C NCBI36
NG_012933.1:g.5429A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.45A>G MANE Select ENSP00000235345.5:p.Glu15=
ENST00000235345.5:c.45A>G ENSP00000235345.5:p.Glu15=
NM_015139.2:c.45A>G NP_055954.1:p.Glu15=
XM_006710478.1:c.45A>G XP_006710541.1:p.Glu15=
XM_011541070.1:c.45A>G XP_011539372.1:p.Glu15=
XM_006710478.2:c.45A>G XP_006710541.1:p.Glu15=
XM_011541070.2:c.45A>G XP_011539372.1:p.Glu15=
XR_001737057.2:n.455A>G
XR_001737058.2:n.448A>G
NM_015139.3:c.45A>G MANE Select NP_055954.1:p.Glu15=