Canonical Allele Identifier: CA1918977659

Gene: CHST3

Linked Data

• dbSNP Id: rs1564533684

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009845_72009846del , CM000672.2:g.72009845_72009846del	GRCh38
NC_000010.10:g.73769603_73769604del , CM000672.1:g.73769603_73769604del	GRCh37
NC_000010.9:g.73439609_73439610del	NCBI36
NG_012635.1:g.50484_50485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1374_*1375del MANE Select	ENSP00000362207.4:n.*1374_*1375del
ENST00000373115.4:c.*1374_*1375del	ENSP00000362207.4:n.*1374_*1375del
NM_004273.4:c.*1374_*1375del	NP_004264.2:n.*1374_*1375del
XM_006718075.2:c.*1374_*1375del	XP_006718138.1:n.*1374_*1375del
XM_011540369.1:c.*1374_*1375del	XP_011538671.1:n.*1374_*1375del
XM_006718075.4:c.*1374_*1375del	XP_006718138.1:n.*1374_*1375del
XM_011540369.2:c.*1374_*1375del	XP_011538671.1:n.*1374_*1375del
NM_004273.5:c.*1374_*1375del MANE Select	NP_004264.2:n.*1374_*1375del