Canonical Allele Identifier: CA344314033

Gene: CHIT1

Linked Data

• MyVariant Identifiers: chr1:g.203194827A>G (hg19) ; chr1:g.203225699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225699A>G , CM000663.2:g.203225699A>G	GRCh38
NC_000001.10:g.203194827A>G , CM000663.1:g.203194827A>G	GRCh37
NC_000001.9:g.201461450A>G	NCBI36
NG_012867.1:g.9034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.227T>C MANE Select	ENSP00000356198.1:p.Leu76Pro
ENST00000255427.7:c.227T>C	ENSP00000255427.3:p.Leu76Pro
ENST00000367229.5:c.227T>C	ENSP00000356198.1:p.Leu76Pro
ENST00000484834.5:n.4584T>C
ENST00000491855.5:c.227T>C	ENSP00000423778.1:p.Leu76Pro
ENST00000503786.1:c.227T>C	ENSP00000421617.1:p.Leu76Pro
ENST00000513472.5:n.423T>C
NM_001256125.1:c.227T>C	NP_001243054.2:p.Leu76Pro
NM_001270509.1:c.227T>C	NP_001257438.1:p.Leu76Pro
NM_003465.2:c.227T>C	NP_003456.1:p.Leu76Pro
NR_045784.1:n.323T>C
NR_045785.1:n.323T>C
XM_011509109.1:c.272T>C	XP_011507411.1:p.Leu91Pro
XM_011509110.1:c.272T>C	XP_011507412.1:p.Leu91Pro
XR_921732.1:n.272T>C
NM_003465.3:c.227T>C MANE Select	NP_003456.1:p.Leu76Pro
NM_001256125.2:c.227T>C	NP_001243054.2:p.Leu76Pro
NR_045784.2:n.264T>C
NR_045785.2:n.264T>C