Canonical Allele Identifier: CA1308854913

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800216A= , CM000664.2:g.174800216A=	GRCh38
NC_000002.11:g.175664944A= , CM000664.1:g.175664944A=	GRCh37
NC_000002.10:g.175373190A=	NCBI36
NG_012642.1:g.210227T=
NG_012642.2:g.210227T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.905T=	ENSP00000295497.7:p.Met302=
ENST00000295497.12:c.905T=	ENSP00000295497.7:p.Met302=
ENST00000409900.9:c.1280T= MANE Select	ENSP00000386741.4:p.Met427=
ENST00000413882.6:c.734T=	ENSP00000410496.2:p.Met245=
ENST00000443238.6:c.758T=	ENSP00000409798.2:p.Met253=
ENST00000488080.6:n.923T=
ENST00000650731.1:c.605T=	ENSP00000499146.1:p.Met202=
ENST00000650938.1:c.666T=
ENST00000651246.1:c.872T=	ENSP00000498484.1:p.Met291=
ENST00000651501.1:c.*727T=	ENSP00000498894.1:n.*727T=
ENST00000651717.1:c.*556T=	ENSP00000499124.1:n.*556T=
ENST00000652036.1:c.956T=	ENSP00000499139.1:p.Met319=
ENST00000295497.11:c.905T=	ENSP00000295497.7:p.Met302=
ENST00000409156.7:c.1202T=	ENSP00000386470.3:p.Met401=
ENST00000409597.5:c.728T=	ENSP00000386469.1:p.Met243=
ENST00000409900.7:c.1280T=	ENSP00000386741.3:p.Met427=
ENST00000488080.5:n.1131T=
ENST00000492964.1:n.423T=
NM_001025201.3:c.1202T=	NP_001020372.2:p.Met401=
NM_001206602.1:c.905T=	NP_001193531.1:p.Met302=
NM_001822.5:c.1280T=	NP_001813.1:p.Met427=
NR_038133.1:n.1146T=
NM_001025201.4:c.1202T=	NP_001020372.2:p.Met401=
NM_001206602.2:c.905T=	NP_001193531.1:p.Met302=
NM_001371513.1:c.1280T=	NP_001358442.1:p.Met427=
NM_001371514.1:c.1331T=	NP_001358443.1:p.Met444=
NM_001822.7:c.1280T= MANE Select	NP_001813.1:p.Met427=
NR_038133.2:n.1148T=