Canonical Allele Identifier: CA1308854979

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800384T= , CM000664.2:g.174800384T=	GRCh38
NC_000002.11:g.175665112T= , CM000664.1:g.175665112T=	GRCh37
NC_000002.10:g.175373358T=	NCBI36
NG_012642.1:g.210059A=
NG_012642.2:g.210059A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-97A=	ENSP00000295497.7:n.834-97A=
ENST00000444394.7:c.963-97A=	ENSP00000411911.2:n.963-97A=
ENST00000295497.12:c.834-97A=	ENSP00000295497.7:n.834-97A=
ENST00000409089.7:c.585-97A=	ENSP00000386322.3:n.585-97A=
ENST00000409900.9:c.1209-97A= MANE Select	ENSP00000386741.4:n.1209-97A=
ENST00000413882.6:c.663-97A=	ENSP00000410496.2:n.663-97A=
ENST00000443238.6:c.687-97A=	ENSP00000409798.2:n.687-97A=
ENST00000444394.6:c.963-97A=	ENSP00000411911.2:n.963-97A=
ENST00000488080.6:n.852-97A=
ENST00000650731.1:c.534-97A=	ENSP00000499146.1:n.534-97A=
ENST00000650938.1:c.595-97A=
ENST00000651246.1:c.801-97A=	ENSP00000498484.1:n.801-97A=
ENST00000651501.1:c.*656-97A=	ENSP00000498894.1:n.*656-97A=
ENST00000651717.1:c.*485-97A=	ENSP00000499124.1:n.*485-97A=
ENST00000652036.1:c.885-97A=	ENSP00000499139.1:n.885-97A=
ENST00000295497.11:c.834-97A=	ENSP00000295497.7:n.834-97A=
ENST00000409156.7:c.1131-97A=	ENSP00000386470.3:n.1131-97A=
ENST00000409597.5:c.657-97A=	ENSP00000386469.1:n.657-97A=
ENST00000409900.7:c.1209-97A=	ENSP00000386741.3:n.1209-97A=
ENST00000488080.5:n.1060-97A=
ENST00000492964.1:n.352-97A=
NM_001025201.3:c.1131-97A=	NP_001020372.2:n.1131-97A=
NM_001206602.1:c.834-97A=	NP_001193531.1:n.834-97A=
NM_001822.5:c.1209-97A=	NP_001813.1:n.1209-97A=
NR_038133.1:n.1075-97A=
NM_001025201.4:c.1131-97A=	NP_001020372.2:n.1131-97A=
NM_001206602.2:c.834-97A=	NP_001193531.1:n.834-97A=
NM_001371513.1:c.1209-97A=	NP_001358442.1:n.1209-97A=
NM_001371514.1:c.1260-97A=	NP_001358443.1:n.1260-97A=
NM_001822.7:c.1209-97A= MANE Select	NP_001813.1:n.1209-97A=
NR_038133.2:n.1077-97A=