Canonical Allele Identifier: CA899173

Gene: SLC35D1

Linked Data

• dbSNP Id: rs775734414
• ExAC: 1:67519585 T / A
• gnomAD v2: 1-67519585-T-A
• gnomAD v4: 1-67053902-T-A
• MyVariant Identifiers: chr1:g.67519585T>A (hg19) ; chr1:g.67053902T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053902T>A , CM000663.2:g.67053902T>A	GRCh38
NC_000001.10:g.67519585T>A , CM000663.1:g.67519585T>A	GRCh37
NC_000001.9:g.67292173T>A	NCBI36
NG_012933.1:g.5496A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.112A>T MANE Select	ENSP00000235345.5:p.Thr38Ser
ENST00000235345.5:c.112A>T	ENSP00000235345.5:p.Thr38Ser
NM_015139.2:c.112A>T	NP_055954.1:p.Thr38Ser
XM_006710478.1:c.112A>T	XP_006710541.1:p.Thr38Ser
XM_011541070.1:c.112A>T	XP_011539372.1:p.Thr38Ser
XM_006710478.2:c.112A>T	XP_006710541.1:p.Thr38Ser
XM_011541070.2:c.112A>T	XP_011539372.1:p.Thr38Ser
XR_001737057.2:n.522A>T
XR_001737058.2:n.515A>T
NM_015139.3:c.112A>T MANE Select	NP_055954.1:p.Thr38Ser