Canonical Allele Identifier: CA380202693

Gene: SLC35C1

Linked Data

• MyVariant Identifiers: chr11:g.45827653G>A (hg19) ; chr11:g.45806102G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806102G>A , CM000673.2:g.45806102G>A	GRCh38
NC_000011.9:g.45827653G>A , CM000673.1:g.45827653G>A	GRCh37
NC_000011.8:g.45784229G>A	NCBI36
NG_009875.1:g.7031G>A , LRG_107:g.7031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.262G>A	ENSP00000432145.2:p.Ala88Thr
ENST00000314134.4:c.301G>A MANE Select	ENSP00000313318.3:p.Ala101Thr
ENST00000314134.3:c.301G>A	ENSP00000313318.3:p.Ala101Thr
ENST00000442528.2:c.262G>A	ENSP00000412408.2:p.Ala88Thr
ENST00000530471.1:c.262G>A	ENSP00000432669.1:p.Ala88Thr
NM_001145265.1:c.262G>A	NP_001138737.1:p.Ala88Thr
NM_001145266.1:c.262G>A	NP_001138738.1:p.Ala88Thr
NM_018389.4:c.301G>A , LRG_107t1:c.301G>A	NP_060859.4:p.Ala101Thr
XM_011520203.1:c.301G>A	XP_011518505.1:p.Ala101Thr
XM_011520203.3:c.301G>A	XP_011518505.1:p.Ala101Thr
NM_001145265.2:c.262G>A	NP_001138737.1:p.Ala88Thr
NM_018389.5:c.301G>A MANE Select	NP_060859.4:p.Ala101Thr