Canonical Allele Identifier: CA1308854927

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800257C= , CM000664.2:g.174800257C=	GRCh38
NC_000002.11:g.175664985C= , CM000664.1:g.175664985C=	GRCh37
NC_000002.10:g.175373231C=	NCBI36
NG_012642.1:g.210186G=
NG_012642.2:g.210186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.864G=	ENSP00000295497.7:p.Met288=
ENST00000295497.12:c.864G=	ENSP00000295497.7:p.Met288=
ENST00000409900.9:c.1239G= MANE Select	ENSP00000386741.4:p.Met413=
ENST00000413882.6:c.693G=	ENSP00000410496.2:p.Met231=
ENST00000443238.6:c.717G=	ENSP00000409798.2:p.Met239=
ENST00000488080.6:n.882G=
ENST00000650731.1:c.564G=	ENSP00000499146.1:p.Met188=
ENST00000650938.1:c.625G=
ENST00000651246.1:c.831G=	ENSP00000498484.1:p.Met277=
ENST00000651501.1:c.*686G=	ENSP00000498894.1:n.*686G=
ENST00000651717.1:c.*515G=	ENSP00000499124.1:n.*515G=
ENST00000652036.1:c.915G=	ENSP00000499139.1:p.Met305=
ENST00000295497.11:c.864G=	ENSP00000295497.7:p.Met288=
ENST00000409156.7:c.1161G=	ENSP00000386470.3:p.Met387=
ENST00000409597.5:c.687G=	ENSP00000386469.1:p.Met229=
ENST00000409900.7:c.1239G=	ENSP00000386741.3:p.Met413=
ENST00000488080.5:n.1090G=
ENST00000492964.1:n.382G=
NM_001025201.3:c.1161G=	NP_001020372.2:p.Met387=
NM_001206602.1:c.864G=	NP_001193531.1:p.Met288=
NM_001822.5:c.1239G=	NP_001813.1:p.Met413=
NR_038133.1:n.1105G=
NM_001025201.4:c.1161G=	NP_001020372.2:p.Met387=
NM_001206602.2:c.864G=	NP_001193531.1:p.Met288=
NM_001371513.1:c.1239G=	NP_001358442.1:p.Met413=
NM_001371514.1:c.1290G=	NP_001358443.1:p.Met430=
NM_001822.7:c.1239G= MANE Select	NP_001813.1:p.Met413=
NR_038133.2:n.1107G=