Canonical Allele Identifier: CA2753244853

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800387_174800388insAGAA , CM000664.2:g.174800387_174800388insAGAA	GRCh38
NC_000002.11:g.175665115_175665116insAGAA , CM000664.1:g.175665115_175665116insAGAA	GRCh37
NC_000002.10:g.175373361_175373362insAGAA	NCBI36
NG_012642.1:g.210055_210056insTTCT
NG_012642.2:g.210055_210056insTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-101_834-100insTTCT	ENSP00000295497.7:n.834-101_834-100insTTCT
ENST00000444394.7:c.963-101_963-100insTTCT	ENSP00000411911.2:n.963-101_963-100insTTCT
ENST00000295497.12:c.834-101_834-100insTTCT	ENSP00000295497.7:n.834-101_834-100insTTCT
ENST00000409089.7:c.585-101_585-100insTTCT	ENSP00000386322.3:n.585-101_585-100insTTCT
ENST00000409900.9:c.1209-101_1209-100insTTCT MANE Select	ENSP00000386741.4:n.1209-101_1209-100insTTCT
ENST00000413882.6:c.663-101_663-100insTTCT	ENSP00000410496.2:n.663-101_663-100insTTCT
ENST00000443238.6:c.687-101_687-100insTTCT	ENSP00000409798.2:n.687-101_687-100insTTCT
ENST00000444394.6:c.963-101_963-100insTTCT	ENSP00000411911.2:n.963-101_963-100insTTCT
ENST00000488080.6:n.852-101_852-100insTTCT
ENST00000650731.1:c.534-101_534-100insTTCT	ENSP00000499146.1:n.534-101_534-100insTTCT
ENST00000650938.1:c.595-101_595-100insTTCT
ENST00000651246.1:c.801-101_801-100insTTCT	ENSP00000498484.1:n.801-101_801-100insTTCT
ENST00000651501.1:c.*656-101_*656-100insTTCT	ENSP00000498894.1:n.*656-101_*656-100insTTCT
ENST00000651717.1:c.*485-101_*485-100insTTCT	ENSP00000499124.1:n.*485-101_*485-100insTTCT
ENST00000652036.1:c.885-101_885-100insTTCT	ENSP00000499139.1:n.885-101_885-100insTTCT
ENST00000295497.11:c.834-101_834-100insTTCT	ENSP00000295497.7:n.834-101_834-100insTTCT
ENST00000409156.7:c.1131-101_1131-100insTTCT	ENSP00000386470.3:n.1131-101_1131-100insTTCT
ENST00000409597.5:c.657-101_657-100insTTCT	ENSP00000386469.1:n.657-101_657-100insTTCT
ENST00000409900.7:c.1209-101_1209-100insTTCT	ENSP00000386741.3:n.1209-101_1209-100insTTCT
ENST00000488080.5:n.1060-101_1060-100insTTCT
ENST00000492964.1:n.352-101_352-100insTTCT
NM_001025201.3:c.1131-101_1131-100insTTCT	NP_001020372.2:n.1131-101_1131-100insTTCT
NM_001206602.1:c.834-101_834-100insTTCT	NP_001193531.1:n.834-101_834-100insTTCT
NM_001822.5:c.1209-101_1209-100insTTCT	NP_001813.1:n.1209-101_1209-100insTTCT
NR_038133.1:n.1075-101_1075-100insTTCT
NM_001025201.4:c.1131-101_1131-100insTTCT	NP_001020372.2:n.1131-101_1131-100insTTCT
NM_001206602.2:c.834-101_834-100insTTCT	NP_001193531.1:n.834-101_834-100insTTCT
NM_001371513.1:c.1209-101_1209-100insTTCT	NP_001358442.1:n.1209-101_1209-100insTTCT
NM_001371514.1:c.1260-101_1260-100insTTCT	NP_001358443.1:n.1260-101_1260-100insTTCT
NM_001822.7:c.1209-101_1209-100insTTCT MANE Select	NP_001813.1:n.1209-101_1209-100insTTCT
NR_038133.2:n.1077-101_1077-100insTTCT