Canonical Allele Identifier: CA422653238

Gene: CHIT1

Linked Data

• MyVariant Identifiers: chr1:g.203194814G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.203225686G>A , CM000663.2:g.203225686G>A	GRCh38
NC_000001.10:g.203194814G>A , CM000663.1:g.203194814G>A	GRCh37
NC_000001.9:g.201461437G>A	NCBI36
NG_012867.1:g.9047C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367229.6:c.240C>T MANE Select	ENSP00000356198.1:p.Phe80=
ENST00000255427.7:c.240C>T	ENSP00000255427.3:p.Phe80=
ENST00000367229.5:c.240C>T	ENSP00000356198.1:p.Phe80=
ENST00000484834.5:n.4597C>T
ENST00000491855.5:c.240C>T	ENSP00000423778.1:p.Phe80=
ENST00000503786.1:c.240C>T	ENSP00000421617.1:p.Phe80=
ENST00000513472.5:n.436C>T
NM_001256125.1:c.240C>T	NP_001243054.2:p.Phe80=
NM_001270509.1:c.240C>T	NP_001257438.1:p.Phe80=
NM_003465.2:c.240C>T	NP_003456.1:p.Phe80=
NR_045784.1:n.336C>T
NR_045785.1:n.336C>T
XM_011509109.1:c.285C>T	XP_011507411.1:p.Phe95=
XM_011509110.1:c.285C>T	XP_011507412.1:p.Phe95=
XR_921732.1:n.285C>T
NM_003465.3:c.240C>T MANE Select	NP_003456.1:p.Phe80=
NM_001256125.2:c.240C>T	NP_001243054.2:p.Phe80=
NR_045784.2:n.277C>T
NR_045785.2:n.277C>T