Canonical Allele Identifier: CA1968693103

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806301_45806304delinsCCTT , CM000673.2:g.45806301_45806304delinsCCTT	GRCh38
NC_000011.9:g.45827852_45827855delinsCCTT , CM000673.1:g.45827852_45827855delinsCCTT	GRCh37
NC_000011.8:g.45784428_45784431delinsCCTT	NCBI36
NG_009875.1:g.7230_7233delinsCCTT , LRG_107:g.7230_7233delinsCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000526817.2:c.461_464delinsCCTT	ENSP00000432145.2:p.Ser154=
ENST00000314134.4:c.500_503delinsCCTT MANE Select	ENSP00000313318.3:p.Ser167=
ENST00000314134.3:c.500_503delinsCCTT	ENSP00000313318.3:p.Ser167=
ENST00000442528.2:c.461_464delinsCCTT	ENSP00000412408.2:p.Ser154=
ENST00000530471.1:c.461_464delinsCCTT	ENSP00000432669.1:p.Ser154=
NM_001145265.1:c.461_464delinsCCTT	NP_001138737.1:p.Ser154=
NM_001145266.1:c.461_464delinsCCTT	NP_001138738.1:p.Ser154=
NM_018389.4:c.500_503delinsCCTT , LRG_107t1:c.500_503delinsCCTT	NP_060859.4:p.Ser167=
XM_011520203.1:c.500_503delinsCCTT	XP_011518505.1:p.Ser167=
XM_011520203.3:c.500_503delinsCCTT	XP_011518505.1:p.Ser167=
NM_001145265.2:c.461_464delinsCCTT	NP_001138737.1:p.Ser154=
NM_018389.5:c.500_503delinsCCTT MANE Select	NP_060859.4:p.Ser167=