Canonical Allele Identifier: CA2481664946

Gene: CHIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225680G= , CM000663.2:g.203225680G=	GRCh38
NC_000001.10:g.203194808G= , CM000663.1:g.203194808G=	GRCh37
NC_000001.9:g.201461431G=	NCBI36
NG_012867.1:g.9053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.246C= MANE Select	ENSP00000356198.1:p.Gly82=
ENST00000255427.7:c.246C=	ENSP00000255427.3:p.Gly82=
ENST00000367229.5:c.246C=	ENSP00000356198.1:p.Gly82=
ENST00000484834.5:n.4603C=
ENST00000491855.5:c.246C=	ENSP00000423778.1:p.Gly82=
ENST00000503786.1:c.246C=	ENSP00000421617.1:p.Gly82=
ENST00000513472.5:n.442C=
NM_001256125.1:c.246C=	NP_001243054.2:p.Gly82=
NM_001270509.1:c.246C=	NP_001257438.1:p.Gly82=
NM_003465.2:c.246C=	NP_003456.1:p.Gly82=
NR_045784.1:n.342C=
NR_045785.1:n.342C=
XM_011509109.1:c.291C=	XP_011507411.1:p.Gly97=
XM_011509110.1:c.291C=	XP_011507412.1:p.Gly97=
XR_921732.1:n.291C=
NM_003465.3:c.246C= MANE Select	NP_003456.1:p.Gly82=
NM_001256125.2:c.246C=	NP_001243054.2:p.Gly82=
NR_045784.2:n.283C=
NR_045785.2:n.283C=