Canonical Allele Identifier: CA898960

Gene: SLC35D1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67047237A>C , CM000663.2:g.67047237A>C	GRCh38
NC_000001.10:g.67512920A>C , CM000663.1:g.67512920A>C	GRCh37
NC_000001.9:g.67285508A>C	NCBI36
NG_012933.1:g.12161T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015139.3:c.636+28T>G MANE Select	NP_055954.1:n.636+28T>G
ENST00000235345.6:c.636+28T>G MANE Select	ENSP00000235345.5:n.636+28T>G
NM_015139.2:c.636+28T>G	NP_055954.1:n.636+28T>G
ENST00000235345.5:c.636+28T>G	ENSP00000235345.5:n.636+28T>G
XM_006710478.1:c.636+28T>G	XP_006710541.1:n.636+28T>G
XM_006710478.2:c.636+28T>G	XP_006710541.1:n.636+28T>G
XM_011541070.1:c.636+28T>G	XP_011539372.1:n.636+28T>G
XM_011541070.2:c.636+28T>G	XP_011539372.1:n.636+28T>G
XR_001737057.2:n.1046+28T>G
XR_001737058.2:n.1039+28T>G
XR_947469.1:n.1172-383A>C