Canonical Allele Identifier: CA2753244877

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800404_174800405insAGAG , CM000664.2:g.174800404_174800405insAGAG	GRCh38
NC_000002.11:g.175665132_175665133insAGAG , CM000664.1:g.175665132_175665133insAGAG	GRCh37
NC_000002.10:g.175373378_175373379insAGAG	NCBI36
NG_012642.1:g.210038_210039insCTCT
NG_012642.2:g.210038_210039insCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.834-118_834-117insCTCT	ENSP00000295497.7:n.834-118_834-117insCTCT
ENST00000444394.7:c.963-118_963-117insCTCT	ENSP00000411911.2:n.963-118_963-117insCTCT
ENST00000295497.12:c.834-118_834-117insCTCT	ENSP00000295497.7:n.834-118_834-117insCTCT
ENST00000409089.7:c.585-118_585-117insCTCT	ENSP00000386322.3:n.585-118_585-117insCTCT
ENST00000409900.9:c.1209-118_1209-117insCTCT MANE Select	ENSP00000386741.4:n.1209-118_1209-117insCTCT
ENST00000413882.6:c.663-118_663-117insCTCT	ENSP00000410496.2:n.663-118_663-117insCTCT
ENST00000443238.6:c.687-118_687-117insCTCT	ENSP00000409798.2:n.687-118_687-117insCTCT
ENST00000444394.6:c.963-118_963-117insCTCT	ENSP00000411911.2:n.963-118_963-117insCTCT
ENST00000488080.6:n.852-118_852-117insCTCT
ENST00000650731.1:c.534-118_534-117insCTCT	ENSP00000499146.1:n.534-118_534-117insCTCT
ENST00000650938.1:c.595-118_595-117insCTCT
ENST00000651246.1:c.801-118_801-117insCTCT	ENSP00000498484.1:n.801-118_801-117insCTCT
ENST00000651501.1:c.*656-118_*656-117insCTCT	ENSP00000498894.1:n.*656-118_*656-117insCTCT
ENST00000651717.1:c.*485-118_*485-117insCTCT	ENSP00000499124.1:n.*485-118_*485-117insCTCT
ENST00000652036.1:c.885-118_885-117insCTCT	ENSP00000499139.1:n.885-118_885-117insCTCT
ENST00000295497.11:c.834-118_834-117insCTCT	ENSP00000295497.7:n.834-118_834-117insCTCT
ENST00000409156.7:c.1131-118_1131-117insCTCT	ENSP00000386470.3:n.1131-118_1131-117insCTCT
ENST00000409597.5:c.657-118_657-117insCTCT	ENSP00000386469.1:n.657-118_657-117insCTCT
ENST00000409900.7:c.1209-118_1209-117insCTCT	ENSP00000386741.3:n.1209-118_1209-117insCTCT
ENST00000488080.5:n.1060-118_1060-117insCTCT
ENST00000492964.1:n.352-118_352-117insCTCT
NM_001025201.3:c.1131-118_1131-117insCTCT	NP_001020372.2:n.1131-118_1131-117insCTCT
NM_001206602.1:c.834-118_834-117insCTCT	NP_001193531.1:n.834-118_834-117insCTCT
NM_001822.5:c.1209-118_1209-117insCTCT	NP_001813.1:n.1209-118_1209-117insCTCT
NR_038133.1:n.1075-118_1075-117insCTCT
NM_001025201.4:c.1131-118_1131-117insCTCT	NP_001020372.2:n.1131-118_1131-117insCTCT
NM_001206602.2:c.834-118_834-117insCTCT	NP_001193531.1:n.834-118_834-117insCTCT
NM_001371513.1:c.1209-118_1209-117insCTCT	NP_001358442.1:n.1209-118_1209-117insCTCT
NM_001371514.1:c.1260-118_1260-117insCTCT	NP_001358443.1:n.1260-118_1260-117insCTCT
NM_001822.7:c.1209-118_1209-117insCTCT MANE Select	NP_001813.1:n.1209-118_1209-117insCTCT
NR_038133.2:n.1077-118_1077-117insCTCT