Canonical Allele Identifier: CA898830

Gene: SLC35D1

Linked Data

• dbSNP Id: rs777118141
• ExAC: 1:67474744 A / G
• gnomAD v2: 1-67474744-A-G
• gnomAD v4: 1-67009061-A-G
• MyVariant Identifiers: chr1:g.67474744A>G (hg19) ; chr1:g.67009061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009061A>G , CM000663.2:g.67009061A>G	GRCh38
NC_000001.10:g.67474744A>G , CM000663.1:g.67474744A>G	GRCh37
NC_000001.9:g.67247332A>G	NCBI36
NG_012933.1:g.50337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.959+24T>C MANE Select	ENSP00000235345.5:n.959+24T>C
ENST00000235345.5:c.959+24T>C	ENSP00000235345.5:n.959+24T>C
NM_015139.2:c.959+24T>C	NP_055954.1:n.959+24T>C
XM_006710478.1:c.1040+24T>C	XP_006710541.1:n.1040+24T>C
XM_011541070.1:c.1040+24T>C	XP_011539372.1:n.1040+24T>C
XM_006710478.2:c.1040+24T>C	XP_006710541.1:n.1040+24T>C
XM_011541070.2:c.1040+24T>C	XP_011539372.1:n.1040+24T>C
XR_001737057.2:n.1543+24T>C
XR_001737058.2:n.2328+24T>C
NM_015139.3:c.959+24T>C MANE Select	NP_055954.1:n.959+24T>C