Canonical Allele Identifier: CA2753244898
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800434_174800435insAC , CM000664.2:g.174800434_174800435insAC GRCh38
NC_000002.11:g.175665162_175665163insAC , CM000664.1:g.175665162_175665163insAC GRCh37
NC_000002.10:g.175373408_175373409insAC NCBI36
NG_012642.1:g.210008_210009insGT
NG_012642.2:g.210008_210009insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.834-148_834-147insGT ENSP00000295497.7:n.834-148_834-147insGT
ENST00000444394.7:c.963-148_963-147insGT ENSP00000411911.2:n.963-148_963-147insGT
ENST00000295497.12:c.834-148_834-147insGT ENSP00000295497.7:n.834-148_834-147insGT
ENST00000409089.7:c.585-148_585-147insGT ENSP00000386322.3:n.585-148_585-147insGT
ENST00000409900.9:c.1209-148_1209-147insGT MANE Select ENSP00000386741.4:n.1209-148_1209-147insGT
ENST00000413882.6:c.663-148_663-147insGT ENSP00000410496.2:n.663-148_663-147insGT
ENST00000443238.6:c.687-148_687-147insGT ENSP00000409798.2:n.687-148_687-147insGT
ENST00000444394.6:c.963-148_963-147insGT ENSP00000411911.2:n.963-148_963-147insGT
ENST00000488080.6:n.852-148_852-147insGT
ENST00000650731.1:c.534-148_534-147insGT ENSP00000499146.1:n.534-148_534-147insGT
ENST00000650938.1:c.595-148_595-147insGT
ENST00000651246.1:c.801-148_801-147insGT ENSP00000498484.1:n.801-148_801-147insGT
ENST00000651501.1:c.*656-148_*656-147insGT ENSP00000498894.1:n.*656-148_*656-147insGT
ENST00000651717.1:c.*485-148_*485-147insGT ENSP00000499124.1:n.*485-148_*485-147insGT
ENST00000652036.1:c.885-148_885-147insGT ENSP00000499139.1:n.885-148_885-147insGT
ENST00000295497.11:c.834-148_834-147insGT ENSP00000295497.7:n.834-148_834-147insGT
ENST00000409156.7:c.1131-148_1131-147insGT ENSP00000386470.3:n.1131-148_1131-147insGT
ENST00000409597.5:c.657-148_657-147insGT ENSP00000386469.1:n.657-148_657-147insGT
ENST00000409900.7:c.1209-148_1209-147insGT ENSP00000386741.3:n.1209-148_1209-147insGT
ENST00000488080.5:n.1060-148_1060-147insGT
ENST00000492964.1:n.352-148_352-147insGT
NM_001025201.3:c.1131-148_1131-147insGT NP_001020372.2:n.1131-148_1131-147insGT
NM_001206602.1:c.834-148_834-147insGT NP_001193531.1:n.834-148_834-147insGT
NM_001822.5:c.1209-148_1209-147insGT NP_001813.1:n.1209-148_1209-147insGT
NR_038133.1:n.1075-148_1075-147insGT
NM_001025201.4:c.1131-148_1131-147insGT NP_001020372.2:n.1131-148_1131-147insGT
NM_001206602.2:c.834-148_834-147insGT NP_001193531.1:n.834-148_834-147insGT
NM_001371513.1:c.1209-148_1209-147insGT NP_001358442.1:n.1209-148_1209-147insGT
NM_001371514.1:c.1260-148_1260-147insGT NP_001358443.1:n.1260-148_1260-147insGT
NM_001822.7:c.1209-148_1209-147insGT MANE Select NP_001813.1:n.1209-148_1209-147insGT
NR_038133.2:n.1077-148_1077-147insGT