Canonical Allele Identifier: CA1308854906

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800193T= , CM000664.2:g.174800193T=	GRCh38
NC_000002.11:g.175664921T= , CM000664.1:g.175664921T=	GRCh37
NC_000002.10:g.175373167T=	NCBI36
NG_012642.1:g.210250A=
NG_012642.2:g.210250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.928A=	ENSP00000295497.7:p.Met310=
ENST00000295497.12:c.928A=	ENSP00000295497.7:p.Met310=
ENST00000409900.9:c.1303A= MANE Select	ENSP00000386741.4:p.Met435=
ENST00000413882.6:c.757A=	ENSP00000410496.2:p.Met253=
ENST00000443238.6:c.781A=	ENSP00000409798.2:p.Met261=
ENST00000488080.6:n.946A=
ENST00000650731.1:c.628A=	ENSP00000499146.1:p.Met210=
ENST00000650938.1:c.689A=
ENST00000651246.1:c.895A=	ENSP00000498484.1:p.Met299=
ENST00000651501.1:c.*750A=	ENSP00000498894.1:n.*750A=
ENST00000651717.1:c.*579A=	ENSP00000499124.1:n.*579A=
ENST00000652036.1:c.979A=	ENSP00000499139.1:p.Met327=
ENST00000295497.11:c.928A=	ENSP00000295497.7:p.Met310=
ENST00000409156.7:c.1225A=	ENSP00000386470.3:p.Met409=
ENST00000409597.5:c.751A=	ENSP00000386469.1:p.Met251=
ENST00000409900.7:c.1303A=	ENSP00000386741.3:p.Met435=
ENST00000488080.5:n.1154A=
ENST00000492964.1:n.446A=
NM_001025201.3:c.1225A=	NP_001020372.2:p.Met409=
NM_001206602.1:c.928A=	NP_001193531.1:p.Met310=
NM_001822.5:c.1303A=	NP_001813.1:p.Met435=
NR_038133.1:n.1169A=
NM_001025201.4:c.1225A=	NP_001020372.2:p.Met409=
NM_001206602.2:c.928A=	NP_001193531.1:p.Met310=
NM_001371513.1:c.1303A=	NP_001358442.1:p.Met435=
NM_001371514.1:c.1354A=	NP_001358443.1:p.Met452=
NM_001822.7:c.1303A= MANE Select	NP_001813.1:p.Met435=
NR_038133.2:n.1171A=