Canonical Allele Identifier: CA380202073

Gene: SLC35C1

Linked Data

• MyVariant Identifiers: chr11:g.45827407G>C (hg19) ; chr11:g.45805856G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805856G>C , CM000673.2:g.45805856G>C	GRCh38
NC_000011.9:g.45827407G>C , CM000673.1:g.45827407G>C	GRCh37
NC_000011.8:g.45783983G>C	NCBI36
NG_009875.1:g.6785G>C , LRG_107:g.6785G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.16G>C	ENSP00000432145.2:p.Ala6Pro
ENST00000314134.4:c.55G>C MANE Select	ENSP00000313318.3:p.Ala19Pro
ENST00000314134.3:c.55G>C	ENSP00000313318.3:p.Ala19Pro
ENST00000442528.2:c.16G>C	ENSP00000412408.2:p.Ala6Pro
ENST00000526817.1:c.16G>C	ENSP00000432145.1:p.Ala6Pro
ENST00000530471.1:c.16G>C	ENSP00000432669.1:p.Ala6Pro
NM_001145265.1:c.16G>C	NP_001138737.1:p.Ala6Pro
NM_001145266.1:c.16G>C	NP_001138738.1:p.Ala6Pro
NM_018389.4:c.55G>C , LRG_107t1:c.55G>C	NP_060859.4:p.Ala19Pro
XM_011520203.1:c.55G>C	XP_011518505.1:p.Ala19Pro
XM_011520203.3:c.55G>C	XP_011518505.1:p.Ala19Pro
NM_001145265.2:c.16G>C	NP_001138737.1:p.Ala6Pro
NM_018389.5:c.55G>C MANE Select	NP_060859.4:p.Ala19Pro