Canonical Allele Identifier: CA1968692930

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806031_45806034delinsCCTT , CM000673.2:g.45806031_45806034delinsCCTT	GRCh38
NC_000011.9:g.45827582_45827585delinsCCTT , CM000673.1:g.45827582_45827585delinsCCTT	GRCh37
NC_000011.8:g.45784158_45784161delinsCCTT	NCBI36
NG_009875.1:g.6960_6963delinsCCTT , LRG_107:g.6960_6963delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.191_194delinsCCTT	ENSP00000432145.2:p.Thr64=
ENST00000314134.4:c.230_233delinsCCTT MANE Select	ENSP00000313318.3:p.Thr77=
ENST00000314134.3:c.230_233delinsCCTT	ENSP00000313318.3:p.Thr77=
ENST00000442528.2:c.191_194delinsCCTT	ENSP00000412408.2:p.Thr64=
ENST00000526817.1:c.191_194delinsCCTT	ENSP00000432145.1:p.Thr64=
ENST00000530471.1:c.191_194delinsCCTT	ENSP00000432669.1:p.Thr64=
NM_001145265.1:c.191_194delinsCCTT	NP_001138737.1:p.Thr64=
NM_001145266.1:c.191_194delinsCCTT	NP_001138738.1:p.Thr64=
NM_018389.4:c.230_233delinsCCTT , LRG_107t1:c.230_233delinsCCTT	NP_060859.4:p.Thr77=
XM_011520203.1:c.230_233delinsCCTT	XP_011518505.1:p.Thr77=
XM_011520203.3:c.230_233delinsCCTT	XP_011518505.1:p.Thr77=
NM_001145265.2:c.191_194delinsCCTT	NP_001138737.1:p.Thr64=
NM_018389.5:c.230_233delinsCCTT MANE Select	NP_060859.4:p.Thr77=