Canonical Allele Identifier: CA2753244867

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800395_174800396insAG , CM000664.2:g.174800395_174800396insAG	GRCh38
NC_000002.11:g.175665123_175665124insAG , CM000664.1:g.175665123_175665124insAG	GRCh37
NC_000002.10:g.175373369_175373370insAG	NCBI36
NG_012642.1:g.210047_210048insCT
NG_012642.2:g.210047_210048insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-109_834-108insCT	ENSP00000295497.7:n.834-109_834-108insCT
ENST00000444394.7:c.963-109_963-108insCT	ENSP00000411911.2:n.963-109_963-108insCT
ENST00000295497.12:c.834-109_834-108insCT	ENSP00000295497.7:n.834-109_834-108insCT
ENST00000409089.7:c.585-109_585-108insCT	ENSP00000386322.3:n.585-109_585-108insCT
ENST00000409900.9:c.1209-109_1209-108insCT MANE Select	ENSP00000386741.4:n.1209-109_1209-108insCT
ENST00000413882.6:c.663-109_663-108insCT	ENSP00000410496.2:n.663-109_663-108insCT
ENST00000443238.6:c.687-109_687-108insCT	ENSP00000409798.2:n.687-109_687-108insCT
ENST00000444394.6:c.963-109_963-108insCT	ENSP00000411911.2:n.963-109_963-108insCT
ENST00000488080.6:n.852-109_852-108insCT
ENST00000650731.1:c.534-109_534-108insCT	ENSP00000499146.1:n.534-109_534-108insCT
ENST00000650938.1:c.595-109_595-108insCT
ENST00000651246.1:c.801-109_801-108insCT	ENSP00000498484.1:n.801-109_801-108insCT
ENST00000651501.1:c.*656-109_*656-108insCT	ENSP00000498894.1:n.*656-109_*656-108insCT
ENST00000651717.1:c.*485-109_*485-108insCT	ENSP00000499124.1:n.*485-109_*485-108insCT
ENST00000652036.1:c.885-109_885-108insCT	ENSP00000499139.1:n.885-109_885-108insCT
ENST00000295497.11:c.834-109_834-108insCT	ENSP00000295497.7:n.834-109_834-108insCT
ENST00000409156.7:c.1131-109_1131-108insCT	ENSP00000386470.3:n.1131-109_1131-108insCT
ENST00000409597.5:c.657-109_657-108insCT	ENSP00000386469.1:n.657-109_657-108insCT
ENST00000409900.7:c.1209-109_1209-108insCT	ENSP00000386741.3:n.1209-109_1209-108insCT
ENST00000488080.5:n.1060-109_1060-108insCT
ENST00000492964.1:n.352-109_352-108insCT
NM_001025201.3:c.1131-109_1131-108insCT	NP_001020372.2:n.1131-109_1131-108insCT
NM_001206602.1:c.834-109_834-108insCT	NP_001193531.1:n.834-109_834-108insCT
NM_001822.5:c.1209-109_1209-108insCT	NP_001813.1:n.1209-109_1209-108insCT
NR_038133.1:n.1075-109_1075-108insCT
NM_001025201.4:c.1131-109_1131-108insCT	NP_001020372.2:n.1131-109_1131-108insCT
NM_001206602.2:c.834-109_834-108insCT	NP_001193531.1:n.834-109_834-108insCT
NM_001371513.1:c.1209-109_1209-108insCT	NP_001358442.1:n.1209-109_1209-108insCT
NM_001371514.1:c.1260-109_1260-108insCT	NP_001358443.1:n.1260-109_1260-108insCT
NM_001822.7:c.1209-109_1209-108insCT MANE Select	NP_001813.1:n.1209-109_1209-108insCT
NR_038133.2:n.1077-109_1077-108insCT