Canonical Allele Identifier: CA221584958

Gene: SLC35C1

Linked Data

• dbSNP Id: rs376096923
• MyVariant Identifiers: chr11:g.45827422_45827427del (hg19) ; chr11:g.45805871_45805876del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805879_45805884del , CM000673.2:g.45805879_45805884del	GRCh38
NC_000011.9:g.45827430_45827435del , CM000673.1:g.45827430_45827435del	GRCh37
NC_000011.8:g.45784006_45784011del	NCBI36
NG_009875.1:g.6808_6813del , LRG_107:g.6808_6813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.39_44del	ENSP00000432145.2:p.Glu14_Ala15del
ENST00000314134.4:c.78_83del MANE Select	ENSP00000313318.3:p.Glu27_Ala28del
ENST00000314134.3:c.78_83del	ENSP00000313318.3:p.Glu27_Ala28del
ENST00000442528.2:c.39_44del	ENSP00000412408.2:p.Glu14_Ala15del
ENST00000526817.1:c.39_44del	ENSP00000432145.1:p.Glu14_Ala15del
ENST00000530471.1:c.39_44del	ENSP00000432669.1:p.Glu14_Ala15del
NM_001145265.1:c.39_44del	NP_001138737.1:p.Glu14_Ala15del
NM_001145266.1:c.39_44del	NP_001138738.1:p.Glu14_Ala15del
NM_018389.4:c.78_83del , LRG_107t1:c.78_83del	NP_060859.4:p.Glu27_Ala28del
XM_011520203.1:c.78_83del	XP_011518505.1:p.Glu27_Ala28del
XM_011520203.3:c.78_83del	XP_011518505.1:p.Glu27_Ala28del
NM_001145265.2:c.39_44del	NP_001138737.1:p.Glu14_Ala15del
NM_018389.5:c.78_83del MANE Select	NP_060859.4:p.Glu27_Ala28del