Canonical Allele Identifier: CA1918977663

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72009856_72009857delinsTC , CM000672.2:g.72009856_72009857delinsTC	GRCh38
NC_000010.10:g.73769614_73769615delinsTC , CM000672.1:g.73769614_73769615delinsTC	GRCh37
NC_000010.9:g.73439620_73439621delinsTC	NCBI36
NG_012635.1:g.50495_50496delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1385_*1386delinsTC MANE Select	ENSP00000362207.4:n.*1385_*1386delinsTC
ENST00000373115.4:c.*1385_*1386delinsTC	ENSP00000362207.4:n.*1385_*1386delinsTC
NM_004273.4:c.*1385_*1386delinsTC	NP_004264.2:n.*1385_*1386delinsTC
XM_006718075.2:c.*1385_*1386delinsTC	XP_006718138.1:n.*1385_*1386delinsTC
XM_011540369.1:c.*1385_*1386delinsTC	XP_011538671.1:n.*1385_*1386delinsTC
XM_006718075.4:c.*1385_*1386delinsTC	XP_006718138.1:n.*1385_*1386delinsTC
XM_011540369.2:c.*1385_*1386delinsTC	XP_011538671.1:n.*1385_*1386delinsTC
NM_004273.5:c.*1385_*1386delinsTC MANE Select	NP_004264.2:n.*1385_*1386delinsTC