Canonical Allele Identifier: CA2753244904

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800442_174800443insACA , CM000664.2:g.174800442_174800443insACA	GRCh38
NC_000002.11:g.175665170_175665171insACA , CM000664.1:g.175665170_175665171insACA	GRCh37
NC_000002.10:g.175373416_175373417insACA	NCBI36
NG_012642.1:g.210000_210001insTGT
NG_012642.2:g.210000_210001insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-156_834-155insTGT	ENSP00000295497.7:n.834-156_834-155insTGT
ENST00000444394.7:c.963-156_963-155insTGT	ENSP00000411911.2:n.963-156_963-155insTGT
ENST00000295497.12:c.834-156_834-155insTGT	ENSP00000295497.7:n.834-156_834-155insTGT
ENST00000409089.7:c.585-156_585-155insTGT	ENSP00000386322.3:n.585-156_585-155insTGT
ENST00000409900.9:c.1209-156_1209-155insTGT MANE Select	ENSP00000386741.4:n.1209-156_1209-155insTGT
ENST00000413882.6:c.663-156_663-155insTGT	ENSP00000410496.2:n.663-156_663-155insTGT
ENST00000443238.6:c.687-156_687-155insTGT	ENSP00000409798.2:n.687-156_687-155insTGT
ENST00000444394.6:c.963-156_963-155insTGT	ENSP00000411911.2:n.963-156_963-155insTGT
ENST00000488080.6:n.852-156_852-155insTGT
ENST00000650731.1:c.534-156_534-155insTGT	ENSP00000499146.1:n.534-156_534-155insTGT
ENST00000650938.1:c.595-156_595-155insTGT
ENST00000651246.1:c.801-156_801-155insTGT	ENSP00000498484.1:n.801-156_801-155insTGT
ENST00000651501.1:c.*656-156_*656-155insTGT	ENSP00000498894.1:n.*656-156_*656-155insTGT
ENST00000651717.1:c.*485-156_*485-155insTGT	ENSP00000499124.1:n.*485-156_*485-155insTGT
ENST00000652036.1:c.885-156_885-155insTGT	ENSP00000499139.1:n.885-156_885-155insTGT
ENST00000295497.11:c.834-156_834-155insTGT	ENSP00000295497.7:n.834-156_834-155insTGT
ENST00000409156.7:c.1131-156_1131-155insTGT	ENSP00000386470.3:n.1131-156_1131-155insTGT
ENST00000409597.5:c.657-156_657-155insTGT	ENSP00000386469.1:n.657-156_657-155insTGT
ENST00000409900.7:c.1209-156_1209-155insTGT	ENSP00000386741.3:n.1209-156_1209-155insTGT
ENST00000488080.5:n.1060-156_1060-155insTGT
ENST00000492964.1:n.352-156_352-155insTGT
NM_001025201.3:c.1131-156_1131-155insTGT	NP_001020372.2:n.1131-156_1131-155insTGT
NM_001206602.1:c.834-156_834-155insTGT	NP_001193531.1:n.834-156_834-155insTGT
NM_001822.5:c.1209-156_1209-155insTGT	NP_001813.1:n.1209-156_1209-155insTGT
NR_038133.1:n.1075-156_1075-155insTGT
NM_001025201.4:c.1131-156_1131-155insTGT	NP_001020372.2:n.1131-156_1131-155insTGT
NM_001206602.2:c.834-156_834-155insTGT	NP_001193531.1:n.834-156_834-155insTGT
NM_001371513.1:c.1209-156_1209-155insTGT	NP_001358442.1:n.1209-156_1209-155insTGT
NM_001371514.1:c.1260-156_1260-155insTGT	NP_001358443.1:n.1260-156_1260-155insTGT
NM_001822.7:c.1209-156_1209-155insTGT MANE Select	NP_001813.1:n.1209-156_1209-155insTGT
NR_038133.2:n.1077-156_1077-155insTGT