Canonical Allele Identifier: CA2753244878
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800408_174800409insA , CM000664.2:g.174800408_174800409insA GRCh38
NC_000002.11:g.175665136_175665137insA , CM000664.1:g.175665136_175665137insA GRCh37
NC_000002.10:g.175373382_175373383insA NCBI36
NG_012642.1:g.210034_210035insT
NG_012642.2:g.210034_210035insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.834-122_834-121insT ENSP00000295497.7:n.834-122_834-121insT
ENST00000444394.7:c.963-122_963-121insT ENSP00000411911.2:n.963-122_963-121insT
ENST00000295497.12:c.834-122_834-121insT ENSP00000295497.7:n.834-122_834-121insT
ENST00000409089.7:c.585-122_585-121insT ENSP00000386322.3:n.585-122_585-121insT
ENST00000409900.9:c.1209-122_1209-121insT MANE Select ENSP00000386741.4:n.1209-122_1209-121insT
ENST00000413882.6:c.663-122_663-121insT ENSP00000410496.2:n.663-122_663-121insT
ENST00000443238.6:c.687-122_687-121insT ENSP00000409798.2:n.687-122_687-121insT
ENST00000444394.6:c.963-122_963-121insT ENSP00000411911.2:n.963-122_963-121insT
ENST00000488080.6:n.852-122_852-121insT
ENST00000650731.1:c.534-122_534-121insT ENSP00000499146.1:n.534-122_534-121insT
ENST00000650938.1:c.595-122_595-121insT
ENST00000651246.1:c.801-122_801-121insT ENSP00000498484.1:n.801-122_801-121insT
ENST00000651501.1:c.*656-122_*656-121insT ENSP00000498894.1:n.*656-122_*656-121insT
ENST00000651717.1:c.*485-122_*485-121insT ENSP00000499124.1:n.*485-122_*485-121insT
ENST00000652036.1:c.885-122_885-121insT ENSP00000499139.1:n.885-122_885-121insT
ENST00000295497.11:c.834-122_834-121insT ENSP00000295497.7:n.834-122_834-121insT
ENST00000409156.7:c.1131-122_1131-121insT ENSP00000386470.3:n.1131-122_1131-121insT
ENST00000409597.5:c.657-122_657-121insT ENSP00000386469.1:n.657-122_657-121insT
ENST00000409900.7:c.1209-122_1209-121insT ENSP00000386741.3:n.1209-122_1209-121insT
ENST00000488080.5:n.1060-122_1060-121insT
ENST00000492964.1:n.352-122_352-121insT
NM_001025201.3:c.1131-122_1131-121insT NP_001020372.2:n.1131-122_1131-121insT
NM_001206602.1:c.834-122_834-121insT NP_001193531.1:n.834-122_834-121insT
NM_001822.5:c.1209-122_1209-121insT NP_001813.1:n.1209-122_1209-121insT
NR_038133.1:n.1075-122_1075-121insT
NM_001025201.4:c.1131-122_1131-121insT NP_001020372.2:n.1131-122_1131-121insT
NM_001206602.2:c.834-122_834-121insT NP_001193531.1:n.834-122_834-121insT
NM_001371513.1:c.1209-122_1209-121insT NP_001358442.1:n.1209-122_1209-121insT
NM_001371514.1:c.1260-122_1260-121insT NP_001358443.1:n.1260-122_1260-121insT
NM_001822.7:c.1209-122_1209-121insT MANE Select NP_001813.1:n.1209-122_1209-121insT
NR_038133.2:n.1077-122_1077-121insT