Canonical Allele Identifier: CA2753244911

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800451_174800452insACAG , CM000664.2:g.174800451_174800452insACAG	GRCh38
NC_000002.11:g.175665179_175665180insACAG , CM000664.1:g.175665179_175665180insACAG	GRCh37
NC_000002.10:g.175373425_175373426insACAG	NCBI36
NG_012642.1:g.209991_209992insCTGT
NG_012642.2:g.209991_209992insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-165_834-164insCTGT	ENSP00000295497.7:n.834-165_834-164insCTGT
ENST00000444394.7:c.963-165_963-164insCTGT	ENSP00000411911.2:n.963-165_963-164insCTGT
ENST00000295497.12:c.834-165_834-164insCTGT	ENSP00000295497.7:n.834-165_834-164insCTGT
ENST00000409089.7:c.585-165_585-164insCTGT	ENSP00000386322.3:n.585-165_585-164insCTGT
ENST00000409900.9:c.1209-165_1209-164insCTGT MANE Select	ENSP00000386741.4:n.1209-165_1209-164insCTGT
ENST00000413882.6:c.663-165_663-164insCTGT	ENSP00000410496.2:n.663-165_663-164insCTGT
ENST00000443238.6:c.687-165_687-164insCTGT	ENSP00000409798.2:n.687-165_687-164insCTGT
ENST00000444394.6:c.963-165_963-164insCTGT	ENSP00000411911.2:n.963-165_963-164insCTGT
ENST00000488080.6:n.852-165_852-164insCTGT
ENST00000650731.1:c.534-165_534-164insCTGT	ENSP00000499146.1:n.534-165_534-164insCTGT
ENST00000650938.1:c.595-165_595-164insCTGT
ENST00000651246.1:c.801-165_801-164insCTGT	ENSP00000498484.1:n.801-165_801-164insCTGT
ENST00000651501.1:c.*656-165_*656-164insCTGT	ENSP00000498894.1:n.*656-165_*656-164insCTGT
ENST00000651717.1:c.*485-165_*485-164insCTGT	ENSP00000499124.1:n.*485-165_*485-164insCTGT
ENST00000652036.1:c.885-165_885-164insCTGT	ENSP00000499139.1:n.885-165_885-164insCTGT
ENST00000295497.11:c.834-165_834-164insCTGT	ENSP00000295497.7:n.834-165_834-164insCTGT
ENST00000409156.7:c.1131-165_1131-164insCTGT	ENSP00000386470.3:n.1131-165_1131-164insCTGT
ENST00000409597.5:c.657-165_657-164insCTGT	ENSP00000386469.1:n.657-165_657-164insCTGT
ENST00000409900.7:c.1209-165_1209-164insCTGT	ENSP00000386741.3:n.1209-165_1209-164insCTGT
ENST00000488080.5:n.1060-165_1060-164insCTGT
ENST00000492964.1:n.352-165_352-164insCTGT
NM_001025201.3:c.1131-165_1131-164insCTGT	NP_001020372.2:n.1131-165_1131-164insCTGT
NM_001206602.1:c.834-165_834-164insCTGT	NP_001193531.1:n.834-165_834-164insCTGT
NM_001822.5:c.1209-165_1209-164insCTGT	NP_001813.1:n.1209-165_1209-164insCTGT
NR_038133.1:n.1075-165_1075-164insCTGT
NM_001025201.4:c.1131-165_1131-164insCTGT	NP_001020372.2:n.1131-165_1131-164insCTGT
NM_001206602.2:c.834-165_834-164insCTGT	NP_001193531.1:n.834-165_834-164insCTGT
NM_001371513.1:c.1209-165_1209-164insCTGT	NP_001358442.1:n.1209-165_1209-164insCTGT
NM_001371514.1:c.1260-165_1260-164insCTGT	NP_001358443.1:n.1260-165_1260-164insCTGT
NM_001822.7:c.1209-165_1209-164insCTGT MANE Select	NP_001813.1:n.1209-165_1209-164insCTGT
NR_038133.2:n.1077-165_1077-164insCTGT