Canonical Allele Identifier: CA899209

Gene: SLC35D1

Linked Data

• dbSNP Id: rs779413390
• ExAC: 1:67519706 A / G
• gnomAD v2: 1-67519706-A-G
• gnomAD v3: 1-67054023-A-G
• gnomAD v4: 1-67054023-A-G
• MyVariant Identifiers: chr1:g.67519706A>G (hg19) ; chr1:g.67054023A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054023A>G , CM000663.2:g.67054023A>G	GRCh38
NC_000001.10:g.67519706A>G , CM000663.1:g.67519706A>G	GRCh37
NC_000001.9:g.67292294A>G	NCBI36
NG_012933.1:g.5375T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-10T>C MANE Select	ENSP00000235345.5:n.-10T>C
ENST00000235345.5:c.-10T>C	ENSP00000235345.5:n.-10T>C
NM_015139.2:c.-10T>C	NP_055954.1:n.-10T>C
XM_006710478.1:c.-10T>C	XP_006710541.1:n.-10T>C
XM_011541070.1:c.-10T>C	XP_011539372.1:n.-10T>C
XM_006710478.2:c.-10T>C	XP_006710541.1:n.-10T>C
XM_011541070.2:c.-10T>C	XP_011539372.1:n.-10T>C
XR_001737057.2:n.401T>C
XR_001737058.2:n.394T>C
NM_015139.3:c.-10T>C MANE Select	NP_055954.1:n.-10T>C