Canonical Allele Identifier: CA2695213700

Gene: SLC35C1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805978_45805980del , CM000673.2:g.45805978_45805980del	GRCh38
NC_000011.9:g.45827529_45827531del , CM000673.1:g.45827529_45827531del	GRCh37
NC_000011.8:g.45784105_45784107del	NCBI36
NG_009875.1:g.6907_6909del , LRG_107:g.6907_6909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.138_140del	ENSP00000432145.2:p.Asn46del
ENST00000314134.4:c.177_179del MANE Select	ENSP00000313318.3:p.Asn59del
ENST00000314134.3:c.177_179del	ENSP00000313318.3:p.Asn59del
ENST00000442528.2:c.138_140del	ENSP00000412408.2:p.Asn46del
ENST00000526817.1:c.138_140del	ENSP00000432145.1:p.Asn46del
ENST00000530471.1:c.138_140del	ENSP00000432669.1:p.Asn46del
NM_001145265.1:c.138_140del	NP_001138737.1:p.Asn46del
NM_001145266.1:c.138_140del	NP_001138738.1:p.Asn46del
NM_018389.4:c.177_179del , LRG_107t1:c.177_179del	NP_060859.4:p.Asn59del
XM_011520203.1:c.177_179del	XP_011518505.1:p.Asn59del
XM_011520203.3:c.177_179del	XP_011518505.1:p.Asn59del
NM_001145265.2:c.138_140del	NP_001138737.1:p.Asn46del
NM_018389.5:c.177_179del MANE Select	NP_060859.4:p.Asn59del