Canonical Allele Identifier: CA24005554

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1004039392
• MyVariant Identifiers: chr1:g.67475014T>A (hg19) ; chr1:g.67009331T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009331T>A , CM000663.2:g.67009331T>A	GRCh38
NC_000001.10:g.67475014T>A , CM000663.1:g.67475014T>A	GRCh37
NC_000001.9:g.67247602T>A	NCBI36
NG_012933.1:g.50067A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-164A>T MANE Select	ENSP00000235345.5:n.877-164A>T
ENST00000235345.5:c.877-164A>T	ENSP00000235345.5:n.877-164A>T
NM_015139.2:c.877-164A>T	NP_055954.1:n.877-164A>T
XM_006710478.1:c.958-164A>T	XP_006710541.1:n.958-164A>T
XM_011541070.1:c.958-164A>T	XP_011539372.1:n.958-164A>T
XM_006710478.2:c.958-164A>T	XP_006710541.1:n.958-164A>T
XM_011541070.2:c.958-164A>T	XP_011539372.1:n.958-164A>T
XR_001737057.2:n.1461-164A>T
XR_001737058.2:n.2246-164A>T
NM_015139.3:c.877-164A>T MANE Select	NP_055954.1:n.877-164A>T