Canonical Allele Identifier: CA738078799

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1222974653
• gnomAD v4: 1-67054099-G-C
• MyVariant Identifiers: chr1:g.67519782G>C (hg19) ; chr1:g.67054099G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054099G>C , CM000663.2:g.67054099G>C	GRCh38
NC_000001.10:g.67519782G>C , CM000663.1:g.67519782G>C	GRCh37
NC_000001.9:g.67292370G>C	NCBI36
NG_012933.1:g.5299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-86C>G MANE Select	ENSP00000235345.5:n.-86C>G
ENST00000235345.5:c.-86C>G	ENSP00000235345.5:n.-86C>G
NM_015139.2:c.-86C>G	NP_055954.1:n.-86C>G
XM_006710478.1:c.-86C>G	XP_006710541.1:n.-86C>G
XM_011541070.1:c.-86C>G	XP_011539372.1:n.-86C>G
XM_006710478.2:c.-86C>G	XP_006710541.1:n.-86C>G
XM_011541070.2:c.-86C>G	XP_011539372.1:n.-86C>G
XR_001737057.2:n.325C>G
XR_001737058.2:n.318C>G
NM_015139.3:c.-86C>G MANE Select	NP_055954.1:n.-86C>G