Canonical Allele Identifier: CA1143885112

Gene: CHIT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225628C= , CM000663.2:g.203225628C=	GRCh38
NC_000001.10:g.203194756C= , CM000663.1:g.203194756C=	GRCh37
NC_000001.9:g.201461379C=	NCBI36
NG_012867.1:g.9105G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.257+41G= MANE Select	ENSP00000356198.1:n.257+41G=
ENST00000255427.7:c.257+41G=	ENSP00000255427.3:n.257+41G=
ENST00000367229.5:c.257+41G=	ENSP00000356198.1:n.257+41G=
ENST00000484834.5:n.4614+41G=
ENST00000491855.5:c.257+41G=	ENSP00000423778.1:n.257+41G=
ENST00000503786.1:c.257+41G=	ENSP00000421617.1:n.257+41G=
ENST00000513472.5:n.453+41G=
NM_001256125.1:c.257+41G=	NP_001243054.2:n.257+41G=
NM_001270509.1:c.257+41G=	NP_001257438.1:n.257+41G=
NM_003465.2:c.257+41G=	NP_003456.1:n.257+41G=
NR_045784.1:n.353+41G=
NR_045785.1:n.353+41G=
XM_011509109.1:c.302+41G=	XP_011507411.1:n.302+41G=
XM_011509110.1:c.302+41G=	XP_011507412.1:n.302+41G=
XR_921732.1:n.302+41G=
NM_003465.3:c.257+41G= MANE Select	NP_003456.1:n.257+41G=
NM_001256125.2:c.257+41G=	NP_001243054.2:n.257+41G=
NR_045784.2:n.294+41G=
NR_045785.2:n.294+41G=