Canonical Allele Identifier: CA2753244840

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800295_174800296insAAAAAAAAA , CM000664.2:g.174800295_174800296insAAAAAAAAA	GRCh38
NC_000002.11:g.175665023_175665024insAAAAAAAAA , CM000664.1:g.175665023_175665024insAAAAAAAAA	GRCh37
NC_000002.10:g.175373269_175373270insAAAAAAAAA	NCBI36
NG_012642.1:g.210152_210153insTTTTTTTTT
NG_012642.2:g.210152_210153insTTTTTTTTT

Transcript Alleles

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