Canonical Allele Identifier: CA1968692962

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806055C= , CM000673.2:g.45806055C=	GRCh38
NC_000011.9:g.45827606C= , CM000673.1:g.45827606C=	GRCh37
NC_000011.8:g.45784182C=	NCBI36
NG_009875.1:g.6984C= , LRG_107:g.6984C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.215C=	ENSP00000432145.2:p.Thr72=
ENST00000314134.4:c.254C= MANE Select	ENSP00000313318.3:p.Thr85=
ENST00000314134.3:c.254C=	ENSP00000313318.3:p.Thr85=
ENST00000442528.2:c.215C=	ENSP00000412408.2:p.Thr72=
ENST00000526817.1:c.215C=	ENSP00000432145.1:p.Thr72=
ENST00000530471.1:c.215C=	ENSP00000432669.1:p.Thr72=
NM_001145265.1:c.215C=	NP_001138737.1:p.Thr72=
NM_001145266.1:c.215C=	NP_001138738.1:p.Thr72=
NM_018389.4:c.254C= , LRG_107t1:c.254C=	NP_060859.4:p.Thr85=
XM_011520203.1:c.254C=	XP_011518505.1:p.Thr85=
XM_011520203.3:c.254C=	XP_011518505.1:p.Thr85=
NM_001145265.2:c.215C=	NP_001138737.1:p.Thr72=
NM_018389.5:c.254C= MANE Select	NP_060859.4:p.Thr85=