Canonical Allele Identifier: CA349347860

Gene: CHN1

Linked Data

• COSMIC: COSM3714046 ; COSM3714047
• MyVariant Identifiers: chr2:g.175689216C>T (hg19) ; chr2:g.174824488C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824488C>T , CM000664.2:g.174824488C>T	GRCh38
NC_000002.11:g.175689216C>T , CM000664.1:g.175689216C>T	GRCh37
NC_000002.10:g.175397462C>T	NCBI36
NG_012642.1:g.185955G>A
NG_012642.2:g.185955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.283G>A	ENSP00000295497.7:p.Glu95Lys
ENST00000444394.7:c.283G>A	ENSP00000411911.2:p.Glu95Lys
ENST00000295497.12:c.283G>A	ENSP00000295497.7:p.Glu95Lys
ENST00000409089.7:c.-18G>A	ENSP00000386322.3:n.-18G>A
ENST00000409900.9:c.658G>A MANE Select	ENSP00000386741.4:p.Glu220Lys
ENST00000413882.6:c.112G>A	ENSP00000410496.2:p.Glu38Lys
ENST00000425395.6:c.*105G>A	ENSP00000405270.2:n.*105G>A
ENST00000443238.6:c.136G>A	ENSP00000409798.2:p.Glu46Lys
ENST00000444394.6:c.283G>A	ENSP00000411911.2:p.Glu95Lys
ENST00000444573.2:c.502G>A	ENSP00000392603.2:p.Glu168Lys
ENST00000488080.6:n.301G>A
ENST00000650731.1:c.-18G>A	ENSP00000499146.1:n.-18G>A
ENST00000650938.1:c.182G>A
ENST00000651246.1:c.250G>A	ENSP00000498484.1:p.Glu84Lys
ENST00000651373.1:c.172G>A	ENSP00000499174.1:p.Glu58Lys
ENST00000651501.1:c.*105G>A	ENSP00000498894.1:n.*105G>A
ENST00000651717.1:c.253-12006G>A	ENSP00000499124.1:n.253-12006G>A
ENST00000652036.1:c.283G>A	ENSP00000499139.1:p.Glu95Lys
ENST00000652154.1:n.556G>A
ENST00000295497.11:c.283G>A	ENSP00000295497.7:p.Glu95Lys
ENST00000409089.6:c.-18G>A	ENSP00000386322.2:n.-18G>A
ENST00000409156.7:c.580G>A	ENSP00000386470.3:p.Glu194Lys
ENST00000409597.5:c.106G>A	ENSP00000386469.1:p.Glu36Lys
ENST00000409900.7:c.658G>A	ENSP00000386741.3:p.Glu220Lys
ENST00000413882.5:c.112G>A	ENSP00000410496.1:p.Glu38Lys
ENST00000425395.5:c.*209G>A	ENSP00000405270.1:n.*209G>A
ENST00000443238.5:c.136G>A	ENSP00000409798.1:p.Glu46Lys
ENST00000444394.5:c.-18G>A	ENSP00000411911.1:n.-18G>A
ENST00000444573.1:c.283G>A	ENSP00000392603.1:p.Glu95Lys
ENST00000485882.1:n.117G>A
ENST00000488080.5:n.509G>A
NM_001025201.3:c.580G>A	NP_001020372.2:p.Glu194Lys
NM_001206602.1:c.283G>A	NP_001193531.1:p.Glu95Lys
NM_001822.5:c.658G>A	NP_001813.1:p.Glu220Lys
NR_038133.1:n.524G>A
NM_001025201.4:c.580G>A	NP_001020372.2:p.Glu194Lys
NM_001206602.2:c.283G>A	NP_001193531.1:p.Glu95Lys
NM_001371513.1:c.658G>A	NP_001358442.1:p.Glu220Lys
NM_001371514.1:c.709G>A	NP_001358443.1:p.Glu237Lys
NM_001822.7:c.658G>A MANE Select	NP_001813.1:p.Glu220Lys
NR_038133.2:n.526G>A