Canonical Allele Identifier: CA1308854772

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799924C= , CM000664.2:g.174799924C=	GRCh38
NC_000002.11:g.175664652C= , CM000664.1:g.175664652C=	GRCh37
NC_000002.10:g.175372898C=	NCBI36
NG_012642.1:g.210519G=
NG_012642.2:g.210519G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*192G=	ENSP00000295497.7:n.*192G=
ENST00000295497.12:c.*192G=	ENSP00000295497.7:n.*192G=
ENST00000409900.9:c.*192G= MANE Select	ENSP00000386741.4:n.*192G=
ENST00000413882.6:c.*192G=	ENSP00000410496.2:n.*192G=
ENST00000443238.6:c.*192G=	ENSP00000409798.2:n.*192G=
ENST00000488080.6:n.1215G=
ENST00000650731.1:c.*192G=	ENSP00000499146.1:n.*192G=
ENST00000650938.1:c.958G=
ENST00000651246.1:c.*192G=	ENSP00000498484.1:n.*192G=
ENST00000651501.1:c.*1019G=	ENSP00000498894.1:n.*1019G=
ENST00000651717.1:c.*848G=	ENSP00000499124.1:n.*848G=
ENST00000652036.1:c.*192G=	ENSP00000499139.1:n.*192G=
ENST00000295497.11:c.*192G=	ENSP00000295497.7:n.*192G=
ENST00000409597.5:c.*192G=	ENSP00000386469.1:n.*192G=
ENST00000409900.7:c.*192G=	ENSP00000386741.3:n.*192G=
ENST00000488080.5:n.1423G=
ENST00000492964.1:n.715G=
NM_001025201.3:c.*192G=	NP_001020372.2:n.*192G=
NM_001206602.1:c.*192G=	NP_001193531.1:n.*192G=
NM_001822.5:c.*192G=	NP_001813.1:n.*192G=
NR_038133.1:n.1438G=
NM_001025201.4:c.*192G=	NP_001020372.2:n.*192G=
NM_001206602.2:c.*192G=	NP_001193531.1:n.*192G=
NM_001371513.1:c.*192G=	NP_001358442.1:n.*192G=
NM_001371514.1:c.*192G=	NP_001358443.1:n.*192G=
NM_001822.7:c.*192G= MANE Select	NP_001813.1:n.*192G=
NR_038133.2:n.1440G=