Canonical Allele Identifier: CA1308854751

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799890T= , CM000664.2:g.174799890T=	GRCh38
NC_000002.11:g.175664618T= , CM000664.1:g.175664618T=	GRCh37
NC_000002.10:g.175372864T=	NCBI36
NG_012642.1:g.210553A=
NG_012642.2:g.210553A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*226A=	ENSP00000295497.7:n.*226A=
ENST00000295497.12:c.*226A=	ENSP00000295497.7:n.*226A=
ENST00000409900.9:c.*226A= MANE Select	ENSP00000386741.4:n.*226A=
ENST00000413882.6:c.*226A=	ENSP00000410496.2:n.*226A=
ENST00000443238.6:c.*226A=	ENSP00000409798.2:n.*226A=
ENST00000488080.6:n.1249A=
ENST00000650731.1:c.*226A=	ENSP00000499146.1:n.*226A=
ENST00000650938.1:c.992A=
ENST00000651246.1:c.*226A=	ENSP00000498484.1:n.*226A=
ENST00000651501.1:c.*1053A=	ENSP00000498894.1:n.*1053A=
ENST00000651717.1:c.*882A=	ENSP00000499124.1:n.*882A=
ENST00000652036.1:c.*226A=	ENSP00000499139.1:n.*226A=
ENST00000295497.11:c.*226A=	ENSP00000295497.7:n.*226A=
ENST00000409597.5:c.*226A=	ENSP00000386469.1:n.*226A=
ENST00000409900.7:c.*226A=	ENSP00000386741.3:n.*226A=
ENST00000488080.5:n.1457A=
NM_001025201.3:c.*226A=	NP_001020372.2:n.*226A=
NM_001206602.1:c.*226A=	NP_001193531.1:n.*226A=
NM_001822.5:c.*226A=	NP_001813.1:n.*226A=
NR_038133.1:n.1472A=
NM_001025201.4:c.*226A=	NP_001020372.2:n.*226A=
NM_001206602.2:c.*226A=	NP_001193531.1:n.*226A=
NM_001371513.1:c.*226A=	NP_001358442.1:n.*226A=
NM_001371514.1:c.*226A=	NP_001358443.1:n.*226A=
NM_001822.7:c.*226A= MANE Select	NP_001813.1:n.*226A=
NR_038133.2:n.1474A=