Canonical Allele Identifier: CA344313912

Gene: CHIT1

Linked Data

• MyVariant Identifiers: chr1:g.203194798T>G (hg19) ; chr1:g.203225670T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225670T>G , CM000663.2:g.203225670T>G	GRCh38
NC_000001.10:g.203194798T>G , CM000663.1:g.203194798T>G	GRCh37
NC_000001.9:g.201461421T>G	NCBI36
NG_012867.1:g.9063A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.256A>C MANE Select	ENSP00000356198.1:p.Met86Leu
ENST00000255427.7:c.256A>C	ENSP00000255427.3:p.Met86Leu
ENST00000367229.5:c.256A>C	ENSP00000356198.1:p.Met86Leu
ENST00000484834.5:n.4613A>C
ENST00000491855.5:c.256A>C	ENSP00000423778.1:p.Met86Leu
ENST00000503786.1:c.256A>C	ENSP00000421617.1:p.Met86Leu
ENST00000513472.5:n.452A>C
NM_001256125.1:c.256A>C	NP_001243054.2:p.Met86Leu
NM_001270509.1:c.256A>C	NP_001257438.1:p.Met86Leu
NM_003465.2:c.256A>C	NP_003456.1:p.Met86Leu
NR_045784.1:n.352A>C
NR_045785.1:n.352A>C
XM_011509109.1:c.301A>C	XP_011507411.1:p.Met101Leu
XM_011509110.1:c.301A>C	XP_011507412.1:p.Met101Leu
XR_921732.1:n.301A>C
NM_003465.3:c.256A>C MANE Select	NP_003456.1:p.Met86Leu
NM_001256125.2:c.256A>C	NP_001243054.2:p.Met86Leu
NR_045784.2:n.293A>C
NR_045785.2:n.293A>C