Canonical Allele Identifier: CA668113017

Gene: CHST3

Linked Data

• dbSNP Id: rs1288519503
• gnomAD v3: 10-72009619-GTGCCCGTGGGGGAGAAGTCCCACCAGGA-G
• gnomAD v4: 10-72009619-GTGCCCGTGGGGGAGAAGTCCCACCAGGA-G
• MyVariant Identifiers: chr10:g.73769378_73769405del (hg19) ; chr10:g.72009620_72009647del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009625_72009652del , CM000672.2:g.72009625_72009652del	GRCh38
NC_000010.10:g.73769383_73769410del , CM000672.1:g.73769383_73769410del	GRCh37
NC_000010.9:g.73439389_73439416del	NCBI36
NG_012635.1:g.50264_50291del

Transcript Alleles

HGVS	Amino-acid change
ENST00000373115.5:c.*1154_*1181del MANE Select	ENSP00000362207.4:n.*1154_*1181del
ENST00000373115.4:c.*1154_*1181del	ENSP00000362207.4:n.*1154_*1181del
NM_004273.4:c.*1154_*1181del	NP_004264.2:n.*1154_*1181del
XM_006718075.2:c.*1154_*1181del	XP_006718138.1:n.*1154_*1181del
XM_011540369.1:c.*1154_*1181del	XP_011538671.1:n.*1154_*1181del
XM_006718075.4:c.*1154_*1181del	XP_006718138.1:n.*1154_*1181del
XM_011540369.2:c.*1154_*1181del	XP_011538671.1:n.*1154_*1181del
NM_004273.5:c.*1154_*1181del MANE Select	NP_004264.2:n.*1154_*1181del