Canonical Allele Identifier: CA1918977799

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010145_72010146delinsTC , CM000672.2:g.72010145_72010146delinsTC	GRCh38
NC_000010.10:g.73769903_73769904delinsTC , CM000672.1:g.73769903_73769904delinsTC	GRCh37
NC_000010.9:g.73439909_73439910delinsTC	NCBI36
NG_012635.1:g.50784_50785delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1674_*1675delinsTC MANE Select	ENSP00000362207.4:n.*1674_*1675delinsTC
ENST00000373115.4:c.*1674_*1675delinsTC	ENSP00000362207.4:n.*1674_*1675delinsTC
NM_004273.4:c.*1674_*1675delinsTC	NP_004264.2:n.*1674_*1675delinsTC
XM_006718075.2:c.*1674_*1675delinsTC	XP_006718138.1:n.*1674_*1675delinsTC
XM_011540369.1:c.*1674_*1675delinsTC	XP_011538671.1:n.*1674_*1675delinsTC
XM_006718075.4:c.*1674_*1675delinsTC	XP_006718138.1:n.*1674_*1675delinsTC
XM_011540369.2:c.*1674_*1675delinsTC	XP_011538671.1:n.*1674_*1675delinsTC
NM_004273.5:c.*1674_*1675delinsTC MANE Select	NP_004264.2:n.*1674_*1675delinsTC