Canonical Allele Identifier: CA2753244889

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800420_174800421insAGA , CM000664.2:g.174800420_174800421insAGA	GRCh38
NC_000002.11:g.175665148_175665149insAGA , CM000664.1:g.175665148_175665149insAGA	GRCh37
NC_000002.10:g.175373394_175373395insAGA	NCBI36
NG_012642.1:g.210022_210023insTCT
NG_012642.2:g.210022_210023insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-134_834-133insTCT	ENSP00000295497.7:n.834-134_834-133insTCT
ENST00000444394.7:c.963-134_963-133insTCT	ENSP00000411911.2:n.963-134_963-133insTCT
ENST00000295497.12:c.834-134_834-133insTCT	ENSP00000295497.7:n.834-134_834-133insTCT
ENST00000409089.7:c.585-134_585-133insTCT	ENSP00000386322.3:n.585-134_585-133insTCT
ENST00000409900.9:c.1209-134_1209-133insTCT MANE Select	ENSP00000386741.4:n.1209-134_1209-133insTCT
ENST00000413882.6:c.663-134_663-133insTCT	ENSP00000410496.2:n.663-134_663-133insTCT
ENST00000443238.6:c.687-134_687-133insTCT	ENSP00000409798.2:n.687-134_687-133insTCT
ENST00000444394.6:c.963-134_963-133insTCT	ENSP00000411911.2:n.963-134_963-133insTCT
ENST00000488080.6:n.852-134_852-133insTCT
ENST00000650731.1:c.534-134_534-133insTCT	ENSP00000499146.1:n.534-134_534-133insTCT
ENST00000650938.1:c.595-134_595-133insTCT
ENST00000651246.1:c.801-134_801-133insTCT	ENSP00000498484.1:n.801-134_801-133insTCT
ENST00000651501.1:c.*656-134_*656-133insTCT	ENSP00000498894.1:n.*656-134_*656-133insTCT
ENST00000651717.1:c.*485-134_*485-133insTCT	ENSP00000499124.1:n.*485-134_*485-133insTCT
ENST00000652036.1:c.885-134_885-133insTCT	ENSP00000499139.1:n.885-134_885-133insTCT
ENST00000295497.11:c.834-134_834-133insTCT	ENSP00000295497.7:n.834-134_834-133insTCT
ENST00000409156.7:c.1131-134_1131-133insTCT	ENSP00000386470.3:n.1131-134_1131-133insTCT
ENST00000409597.5:c.657-134_657-133insTCT	ENSP00000386469.1:n.657-134_657-133insTCT
ENST00000409900.7:c.1209-134_1209-133insTCT	ENSP00000386741.3:n.1209-134_1209-133insTCT
ENST00000488080.5:n.1060-134_1060-133insTCT
ENST00000492964.1:n.352-134_352-133insTCT
NM_001025201.3:c.1131-134_1131-133insTCT	NP_001020372.2:n.1131-134_1131-133insTCT
NM_001206602.1:c.834-134_834-133insTCT	NP_001193531.1:n.834-134_834-133insTCT
NM_001822.5:c.1209-134_1209-133insTCT	NP_001813.1:n.1209-134_1209-133insTCT
NR_038133.1:n.1075-134_1075-133insTCT
NM_001025201.4:c.1131-134_1131-133insTCT	NP_001020372.2:n.1131-134_1131-133insTCT
NM_001206602.2:c.834-134_834-133insTCT	NP_001193531.1:n.834-134_834-133insTCT
NM_001371513.1:c.1209-134_1209-133insTCT	NP_001358442.1:n.1209-134_1209-133insTCT
NM_001371514.1:c.1260-134_1260-133insTCT	NP_001358443.1:n.1260-134_1260-133insTCT
NM_001822.7:c.1209-134_1209-133insTCT MANE Select	NP_001813.1:n.1209-134_1209-133insTCT
NR_038133.2:n.1077-134_1077-133insTCT