Canonical Allele Identifier: CA523619011

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1289618755
• gnomAD v2: 1-67474748-A-C
• gnomAD v4: 1-67009065-A-C
• MyVariant Identifiers: chr1:g.67474748A>C (hg19) ; chr1:g.67009065A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009065A>C , CM000663.2:g.67009065A>C	GRCh38
NC_000001.10:g.67474748A>C , CM000663.1:g.67474748A>C	GRCh37
NC_000001.9:g.67247336A>C	NCBI36
NG_012933.1:g.50333T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.959+20T>G MANE Select	ENSP00000235345.5:n.959+20T>G
ENST00000235345.5:c.959+20T>G	ENSP00000235345.5:n.959+20T>G
NM_015139.2:c.959+20T>G	NP_055954.1:n.959+20T>G
XM_006710478.1:c.1040+20T>G	XP_006710541.1:n.1040+20T>G
XM_011541070.1:c.1040+20T>G	XP_011539372.1:n.1040+20T>G
XM_006710478.2:c.1040+20T>G	XP_006710541.1:n.1040+20T>G
XM_011541070.2:c.1040+20T>G	XP_011539372.1:n.1040+20T>G
XR_001737057.2:n.1543+20T>G
XR_001737058.2:n.2328+20T>G
NM_015139.3:c.959+20T>G MANE Select	NP_055954.1:n.959+20T>G