Canonical Allele Identifier: CA2753244893
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800424_174800432del , CM000664.2:g.174800424_174800432del GRCh38
NC_000002.11:g.175665152_175665160del , CM000664.1:g.175665152_175665160del GRCh37
NC_000002.10:g.175373398_175373406del NCBI36
NG_012642.1:g.210011_210019del
NG_012642.2:g.210011_210019del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.834-145_834-137del ENSP00000295497.7:n.834-145_834-137del
ENST00000444394.7:c.963-145_963-137del ENSP00000411911.2:n.963-145_963-137del
ENST00000295497.12:c.834-145_834-137del ENSP00000295497.7:n.834-145_834-137del
ENST00000409089.7:c.585-145_585-137del ENSP00000386322.3:n.585-145_585-137del
ENST00000409900.9:c.1209-145_1209-137del MANE Select ENSP00000386741.4:n.1209-145_1209-137del
ENST00000413882.6:c.663-145_663-137del ENSP00000410496.2:n.663-145_663-137del
ENST00000443238.6:c.687-145_687-137del ENSP00000409798.2:n.687-145_687-137del
ENST00000444394.6:c.963-145_963-137del ENSP00000411911.2:n.963-145_963-137del
ENST00000488080.6:n.852-145_852-137del
ENST00000650731.1:c.534-145_534-137del ENSP00000499146.1:n.534-145_534-137del
ENST00000650938.1:c.595-145_595-137del
ENST00000651246.1:c.801-145_801-137del ENSP00000498484.1:n.801-145_801-137del
ENST00000651501.1:c.*656-145_*656-137del ENSP00000498894.1:n.*656-145_*656-137del
ENST00000651717.1:c.*485-145_*485-137del ENSP00000499124.1:n.*485-145_*485-137del
ENST00000652036.1:c.885-145_885-137del ENSP00000499139.1:n.885-145_885-137del
ENST00000295497.11:c.834-145_834-137del ENSP00000295497.7:n.834-145_834-137del
ENST00000409156.7:c.1131-145_1131-137del ENSP00000386470.3:n.1131-145_1131-137del
ENST00000409597.5:c.657-145_657-137del ENSP00000386469.1:n.657-145_657-137del
ENST00000409900.7:c.1209-145_1209-137del ENSP00000386741.3:n.1209-145_1209-137del
ENST00000488080.5:n.1060-145_1060-137del
ENST00000492964.1:n.352-145_352-137del
NM_001025201.3:c.1131-145_1131-137del NP_001020372.2:n.1131-145_1131-137del
NM_001206602.1:c.834-145_834-137del NP_001193531.1:n.834-145_834-137del
NM_001822.5:c.1209-145_1209-137del NP_001813.1:n.1209-145_1209-137del
NR_038133.1:n.1075-145_1075-137del
NM_001025201.4:c.1131-145_1131-137del NP_001020372.2:n.1131-145_1131-137del
NM_001206602.2:c.834-145_834-137del NP_001193531.1:n.834-145_834-137del
NM_001371513.1:c.1209-145_1209-137del NP_001358442.1:n.1209-145_1209-137del
NM_001371514.1:c.1260-145_1260-137del NP_001358443.1:n.1260-145_1260-137del
NM_001822.7:c.1209-145_1209-137del MANE Select NP_001813.1:n.1209-145_1209-137del
NR_038133.2:n.1077-145_1077-137del