Canonical Allele Identifier: CA1918977772

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010060A= , CM000672.2:g.72010060A=	GRCh38
NC_000010.10:g.73769818A= , CM000672.1:g.73769818A=	GRCh37
NC_000010.9:g.73439824A=	NCBI36
NG_012635.1:g.50699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1589A= MANE Select	ENSP00000362207.4:n.*1589A=
ENST00000373115.4:c.*1589A=	ENSP00000362207.4:n.*1589A=
NM_004273.4:c.*1589A=	NP_004264.2:n.*1589A=
XM_006718075.2:c.*1589A=	XP_006718138.1:n.*1589A=
XM_011540369.1:c.*1589A=	XP_011538671.1:n.*1589A=
XM_006718075.4:c.*1589A=	XP_006718138.1:n.*1589A=
XM_011540369.2:c.*1589A=	XP_011538671.1:n.*1589A=
NM_004273.5:c.*1589A= MANE Select	NP_004264.2:n.*1589A=