Canonical Allele Identifier: CA1918977819

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72010181G= , CM000672.2:g.72010181G=	GRCh38
NC_000010.10:g.73769939G= , CM000672.1:g.73769939G=	GRCh37
NC_000010.9:g.73439945G=	NCBI36
NG_012635.1:g.50820G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.*1710G= MANE Select	ENSP00000362207.4:n.*1710G=
ENST00000373115.4:c.*1710G=	ENSP00000362207.4:n.*1710G=
NM_004273.4:c.*1710G=	NP_004264.2:n.*1710G=
XM_006718075.2:c.*1710G=	XP_006718138.1:n.*1710G=
XM_011540369.1:c.*1710G=	XP_011538671.1:n.*1710G=
XM_006718075.4:c.*1710G=	XP_006718138.1:n.*1710G=
XM_011540369.2:c.*1710G=	XP_011538671.1:n.*1710G=
NM_004273.5:c.*1710G= MANE Select	NP_004264.2:n.*1710G=