Canonical Allele Identifier: CA899203

Gene: SLC35D1

Linked Data

• dbSNP Id: rs751348978
• ExAC: 1:67519687 C / A
• gnomAD v2: 1-67519687-C-A
• gnomAD v4: 1-67054004-C-A
• MyVariant Identifiers: chr1:g.67519687C>A (hg19) ; chr1:g.67054004C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054004C>A , CM000663.2:g.67054004C>A	GRCh38
NC_000001.10:g.67519687C>A , CM000663.1:g.67519687C>A	GRCh37
NC_000001.9:g.67292275C>A	NCBI36
NG_012933.1:g.5394G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.10G>T MANE Select	ENSP00000235345.5:p.Val4Phe
ENST00000235345.5:c.10G>T	ENSP00000235345.5:p.Val4Phe
NM_015139.2:c.10G>T	NP_055954.1:p.Val4Phe
XM_006710478.1:c.10G>T	XP_006710541.1:p.Val4Phe
XM_011541070.1:c.10G>T	XP_011539372.1:p.Val4Phe
XM_006710478.2:c.10G>T	XP_006710541.1:p.Val4Phe
XM_011541070.2:c.10G>T	XP_011539372.1:p.Val4Phe
XR_001737057.2:n.420G>T
XR_001737058.2:n.413G>T
NM_015139.3:c.10G>T MANE Select	NP_055954.1:p.Val4Phe