Canonical Allele Identifier: CA1308865703

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824486T= , CM000664.2:g.174824486T=	GRCh38
NC_000002.11:g.175689214T= , CM000664.1:g.175689214T=	GRCh37
NC_000002.10:g.175397460T=	NCBI36
NG_012642.1:g.185957A=
NG_012642.2:g.185957A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.285A=	ENSP00000295497.7:p.Glu95=
ENST00000444394.7:c.285A=	ENSP00000411911.2:p.Glu95=
ENST00000295497.12:c.285A=	ENSP00000295497.7:p.Glu95=
ENST00000409089.7:c.-16A=	ENSP00000386322.3:n.-16A=
ENST00000409900.9:c.660A= MANE Select	ENSP00000386741.4:p.Glu220=
ENST00000413882.6:c.114A=	ENSP00000410496.2:p.Glu38=
ENST00000425395.6:c.*107A=	ENSP00000405270.2:n.*107A=
ENST00000443238.6:c.138A=	ENSP00000409798.2:p.Glu46=
ENST00000444394.6:c.285A=	ENSP00000411911.2:p.Glu95=
ENST00000444573.2:c.504A=	ENSP00000392603.2:p.Glu168=
ENST00000488080.6:n.303A=
ENST00000650731.1:c.-16A=	ENSP00000499146.1:n.-16A=
ENST00000650938.1:c.184A=
ENST00000651246.1:c.252A=	ENSP00000498484.1:p.Glu84=
ENST00000651373.1:c.174A=	ENSP00000499174.1:p.Glu58=
ENST00000651501.1:c.*107A=	ENSP00000498894.1:n.*107A=
ENST00000651717.1:c.253-12004A=	ENSP00000499124.1:n.253-12004A=
ENST00000652036.1:c.285A=	ENSP00000499139.1:p.Glu95=
ENST00000652154.1:n.558A=
ENST00000295497.11:c.285A=	ENSP00000295497.7:p.Glu95=
ENST00000409089.6:c.-16A=	ENSP00000386322.2:n.-16A=
ENST00000409156.7:c.582A=	ENSP00000386470.3:p.Glu194=
ENST00000409597.5:c.108A=	ENSP00000386469.1:p.Glu36=
ENST00000409900.7:c.660A=	ENSP00000386741.3:p.Glu220=
ENST00000413882.5:c.114A=	ENSP00000410496.1:p.Glu38=
ENST00000425395.5:c.*211A=	ENSP00000405270.1:n.*211A=
ENST00000443238.5:c.138A=	ENSP00000409798.1:p.Glu46=
ENST00000444394.5:c.-16A=	ENSP00000411911.1:n.-16A=
ENST00000444573.1:c.285A=	ENSP00000392603.1:p.Glu95=
ENST00000485882.1:n.119A=
ENST00000488080.5:n.511A=
NM_001025201.3:c.582A=	NP_001020372.2:p.Glu194=
NM_001206602.1:c.285A=	NP_001193531.1:p.Glu95=
NM_001822.5:c.660A=	NP_001813.1:p.Glu220=
NR_038133.1:n.526A=
NM_001025201.4:c.582A=	NP_001020372.2:p.Glu194=
NM_001206602.2:c.285A=	NP_001193531.1:p.Glu95=
NM_001371513.1:c.660A=	NP_001358442.1:p.Glu220=
NM_001371514.1:c.711A=	NP_001358443.1:p.Glu237=
NM_001822.7:c.660A= MANE Select	NP_001813.1:p.Glu220=
NR_038133.2:n.528A=