Canonical Allele Identifier: CA1308854554

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799453A= , CM000664.2:g.174799453A=	GRCh38
NC_000002.11:g.175664181A= , CM000664.1:g.175664181A=	GRCh37
NC_000002.10:g.175372427A=	NCBI36
NG_012642.1:g.210990T=
NG_012642.2:g.210990T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*663T=	ENSP00000295497.7:n.*663T=
ENST00000295497.12:c.*663T=	ENSP00000295497.7:n.*663T=
ENST00000409900.9:c.*663T= MANE Select	ENSP00000386741.4:n.*663T=
ENST00000443238.6:c.*663T=	ENSP00000409798.2:n.*663T=
ENST00000652036.1:c.*663T=	ENSP00000499139.1:n.*663T=
ENST00000409900.7:c.*663T=	ENSP00000386741.3:n.*663T=
NM_001025201.3:c.*663T=	NP_001020372.2:n.*663T=
NM_001206602.1:c.*663T=	NP_001193531.1:n.*663T=
NM_001822.5:c.*663T=	NP_001813.1:n.*663T=
NR_038133.1:n.1909T=
NM_001025201.4:c.*663T=	NP_001020372.2:n.*663T=
NM_001206602.2:c.*663T=	NP_001193531.1:n.*663T=
NM_001371513.1:c.*663T=	NP_001358442.1:n.*663T=
NM_001371514.1:c.*663T=	NP_001358443.1:n.*663T=
NM_001822.7:c.*663T= MANE Select	NP_001813.1:n.*663T=
NR_038133.2:n.1911T=