Canonical Allele Identifier: CA2481664954

Gene: CHIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225697A= , CM000663.2:g.203225697A=	GRCh38
NC_000001.10:g.203194825A= , CM000663.1:g.203194825A=	GRCh37
NC_000001.9:g.201461448A=	NCBI36
NG_012867.1:g.9036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.229T= MANE Select	ENSP00000356198.1:p.Tyr77=
ENST00000255427.7:c.229T=	ENSP00000255427.3:p.Tyr77=
ENST00000367229.5:c.229T=	ENSP00000356198.1:p.Tyr77=
ENST00000484834.5:n.4586T=
ENST00000491855.5:c.229T=	ENSP00000423778.1:p.Tyr77=
ENST00000503786.1:c.229T=	ENSP00000421617.1:p.Tyr77=
ENST00000513472.5:n.425T=
NM_001256125.1:c.229T=	NP_001243054.2:p.Tyr77=
NM_001270509.1:c.229T=	NP_001257438.1:p.Tyr77=
NM_003465.2:c.229T=	NP_003456.1:p.Tyr77=
NR_045784.1:n.325T=
NR_045785.1:n.325T=
XM_011509109.1:c.274T=	XP_011507411.1:p.Tyr92=
XM_011509110.1:c.274T=	XP_011507412.1:p.Tyr92=
XR_921732.1:n.274T=
NM_003465.3:c.229T= MANE Select	NP_003456.1:p.Tyr77=
NM_001256125.2:c.229T=	NP_001243054.2:p.Tyr77=
NR_045784.2:n.266T=
NR_045785.2:n.266T=