Canonical Allele Identifier: CA1308854777

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799934G= , CM000664.2:g.174799934G=	GRCh38
NC_000002.11:g.175664662G= , CM000664.1:g.175664662G=	GRCh37
NC_000002.10:g.175372908G=	NCBI36
NG_012642.1:g.210509C=
NG_012642.2:g.210509C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*182C=	ENSP00000295497.7:n.*182C=
ENST00000295497.12:c.*182C=	ENSP00000295497.7:n.*182C=
ENST00000409900.9:c.*182C= MANE Select	ENSP00000386741.4:n.*182C=
ENST00000413882.6:c.*182C=	ENSP00000410496.2:n.*182C=
ENST00000443238.6:c.*182C=	ENSP00000409798.2:n.*182C=
ENST00000488080.6:n.1205C=
ENST00000650731.1:c.*182C=	ENSP00000499146.1:n.*182C=
ENST00000650938.1:c.948C=
ENST00000651246.1:c.*182C=	ENSP00000498484.1:n.*182C=
ENST00000651501.1:c.*1009C=	ENSP00000498894.1:n.*1009C=
ENST00000651717.1:c.*838C=	ENSP00000499124.1:n.*838C=
ENST00000652036.1:c.*182C=	ENSP00000499139.1:n.*182C=
ENST00000295497.11:c.*182C=	ENSP00000295497.7:n.*182C=
ENST00000409597.5:c.*182C=	ENSP00000386469.1:n.*182C=
ENST00000409900.7:c.*182C=	ENSP00000386741.3:n.*182C=
ENST00000488080.5:n.1413C=
ENST00000492964.1:n.705C=
NM_001025201.3:c.*182C=	NP_001020372.2:n.*182C=
NM_001206602.1:c.*182C=	NP_001193531.1:n.*182C=
NM_001822.5:c.*182C=	NP_001813.1:n.*182C=
NR_038133.1:n.1428C=
NM_001025201.4:c.*182C=	NP_001020372.2:n.*182C=
NM_001206602.2:c.*182C=	NP_001193531.1:n.*182C=
NM_001371513.1:c.*182C=	NP_001358442.1:n.*182C=
NM_001371514.1:c.*182C=	NP_001358443.1:n.*182C=
NM_001822.7:c.*182C= MANE Select	NP_001813.1:n.*182C=
NR_038133.2:n.1430C=