Canonical Allele Identifier: CA1140181052

Gene: CHIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203217835C= , CM000663.2:g.203217835C=	GRCh38
NC_000001.10:g.203186963C= , CM000663.1:g.203186963C=	GRCh37
NC_000001.9:g.201453586C=	NCBI36
NG_012867.1:g.16898G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003465.3:c.1060G= MANE Select	NP_003456.1:p.Gly354=
ENST00000367229.6:c.1060G= MANE Select	ENSP00000356198.1:p.Gly354=
NM_001256125.1:c.1003G=	NP_001243054.2:p.Gly335=
NM_001256125.2:c.1003G=	NP_001243054.2:p.Gly335=
NM_001270509.1:c.982-57G=	NP_001257438.1:n.982-57G=
NM_003465.2:c.1060G=	NP_003456.1:p.Gly354=
NR_045784.1:n.1313G=
NR_045784.2:n.1254G=
NR_045785.1:n.1156G=
NR_045785.2:n.1097G=
ENST00000255427.7:c.1003G=	ENSP00000255427.3:p.Gly335=
ENST00000367229.5:c.1060G=	ENSP00000356198.1:p.Gly354=
ENST00000479483.1:n.187G=
ENST00000484834.5:n.5292G=
ENST00000491855.5:c.1060G=	ENSP00000423778.1:p.Gly354=
ENST00000503786.1:c.*131G=	ENSP00000421617.1:n.*131G=
XM_011509109.1:c.1105G=	XP_011507411.1:p.Gly369=
XM_011509110.1:c.1105G=	XP_011507412.1:p.Gly369=
XR_921732.1:n.1262G=