Canonical Allele Identifier: CA1918977350

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009258_72009259delinsAG , CM000672.2:g.72009258_72009259delinsAG	GRCh38
NC_000010.10:g.73769016_73769017delinsAG , CM000672.1:g.73769016_73769017delinsAG	GRCh37
NC_000010.9:g.73439022_73439023delinsAG	NCBI36
NG_012635.1:g.49897_49898delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*787_*788delinsAG MANE Select	ENSP00000362207.4:n.*787_*788delinsAG
ENST00000373115.4:c.*787_*788delinsAG	ENSP00000362207.4:n.*787_*788delinsAG
NM_004273.4:c.*787_*788delinsAG	NP_004264.2:n.*787_*788delinsAG
XM_006718075.2:c.*787_*788delinsAG	XP_006718138.1:n.*787_*788delinsAG
XM_011540369.1:c.*787_*788delinsAG	XP_011538671.1:n.*787_*788delinsAG
XM_006718075.4:c.*787_*788delinsAG	XP_006718138.1:n.*787_*788delinsAG
XM_011540369.2:c.*787_*788delinsAG	XP_011538671.1:n.*787_*788delinsAG
NM_004273.5:c.*787_*788delinsAG MANE Select	NP_004264.2:n.*787_*788delinsAG