Canonical Allele Identifier: CA340708824

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1483494839
• MyVariant Identifiers: chr1:g.67519692G>A (hg19) ; chr1:g.67054009G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054009G>A , CM000663.2:g.67054009G>A	GRCh38
NC_000001.10:g.67519692G>A , CM000663.1:g.67519692G>A	GRCh37
NC_000001.9:g.67292280G>A	NCBI36
NG_012933.1:g.5389C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.5C>T MANE Select	ENSP00000235345.5:p.Ala2Val
ENST00000235345.5:c.5C>T	ENSP00000235345.5:p.Ala2Val
NM_015139.2:c.5C>T	NP_055954.1:p.Ala2Val
XM_006710478.1:c.5C>T	XP_006710541.1:p.Ala2Val
XM_011541070.1:c.5C>T	XP_011539372.1:p.Ala2Val
XM_006710478.2:c.5C>T	XP_006710541.1:p.Ala2Val
XM_011541070.2:c.5C>T	XP_011539372.1:p.Ala2Val
XR_001737057.2:n.415C>T
XR_001737058.2:n.408C>T
NM_015139.3:c.5C>T MANE Select	NP_055954.1:p.Ala2Val