Canonical Allele Identifier: CA2577164037

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800098dup , CM000664.2:g.174800098dup	GRCh38
NC_000002.11:g.175664826dup , CM000664.1:g.175664826dup	GRCh37
NC_000002.10:g.175373072dup	NCBI36
NG_012642.1:g.210348dup
NG_012642.2:g.210348dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*21dup	ENSP00000295497.7:n.*21dup
ENST00000295497.12:c.*21dup	ENSP00000295497.7:n.*21dup
ENST00000409900.9:c.*21dup MANE Select	ENSP00000386741.4:n.*21dup
ENST00000413882.6:c.*21dup	ENSP00000410496.2:n.*21dup
ENST00000443238.6:c.*21dup	ENSP00000409798.2:n.*21dup
ENST00000488080.6:n.1044dup
ENST00000650731.1:c.*21dup	ENSP00000499146.1:n.*21dup
ENST00000650938.1:c.787dup
ENST00000651246.1:c.*21dup	ENSP00000498484.1:n.*21dup
ENST00000651501.1:c.*848dup	ENSP00000498894.1:n.*848dup
ENST00000651717.1:c.*677dup	ENSP00000499124.1:n.*677dup
ENST00000652036.1:c.*21dup	ENSP00000499139.1:n.*21dup
ENST00000295497.11:c.*21dup	ENSP00000295497.7:n.*21dup
ENST00000409156.7:c.*21dup	ENSP00000386470.3:n.*21dup
ENST00000409597.5:c.*21dup	ENSP00000386469.1:n.*21dup
ENST00000409900.7:c.*21dup	ENSP00000386741.3:n.*21dup
ENST00000488080.5:n.1252dup
ENST00000492964.1:n.544dup
NM_001025201.3:c.*21dup	NP_001020372.2:n.*21dup
NM_001206602.1:c.*21dup	NP_001193531.1:n.*21dup
NM_001822.5:c.*21dup	NP_001813.1:n.*21dup
NR_038133.1:n.1267dup
NM_001025201.4:c.*21dup	NP_001020372.2:n.*21dup
NM_001206602.2:c.*21dup	NP_001193531.1:n.*21dup
NM_001371513.1:c.*21dup	NP_001358442.1:n.*21dup
NM_001371514.1:c.*21dup	NP_001358443.1:n.*21dup
NM_001822.7:c.*21dup MANE Select	NP_001813.1:n.*21dup
NR_038133.2:n.1269dup