Canonical Allele Identifier: CA2753244846
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800381_174800382insAGA , CM000664.2:g.174800381_174800382insAGA GRCh38
NC_000002.11:g.175665109_175665110insAGA , CM000664.1:g.175665109_175665110insAGA GRCh37
NC_000002.10:g.175373355_175373356insAGA NCBI36
NG_012642.1:g.210061_210062insTCT
NG_012642.2:g.210061_210062insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.834-95_834-94insTCT ENSP00000295497.7:n.834-95_834-94insTCT
ENST00000444394.7:c.963-95_963-94insTCT ENSP00000411911.2:n.963-95_963-94insTCT
ENST00000295497.12:c.834-95_834-94insTCT ENSP00000295497.7:n.834-95_834-94insTCT
ENST00000409089.7:c.585-95_585-94insTCT ENSP00000386322.3:n.585-95_585-94insTCT
ENST00000409900.9:c.1209-95_1209-94insTCT MANE Select ENSP00000386741.4:n.1209-95_1209-94insTCT
ENST00000413882.6:c.663-95_663-94insTCT ENSP00000410496.2:n.663-95_663-94insTCT
ENST00000443238.6:c.687-95_687-94insTCT ENSP00000409798.2:n.687-95_687-94insTCT
ENST00000444394.6:c.963-95_963-94insTCT ENSP00000411911.2:n.963-95_963-94insTCT
ENST00000488080.6:n.852-95_852-94insTCT
ENST00000650731.1:c.534-95_534-94insTCT ENSP00000499146.1:n.534-95_534-94insTCT
ENST00000650938.1:c.595-95_595-94insTCT
ENST00000651246.1:c.801-95_801-94insTCT ENSP00000498484.1:n.801-95_801-94insTCT
ENST00000651501.1:c.*656-95_*656-94insTCT ENSP00000498894.1:n.*656-95_*656-94insTCT
ENST00000651717.1:c.*485-95_*485-94insTCT ENSP00000499124.1:n.*485-95_*485-94insTCT
ENST00000652036.1:c.885-95_885-94insTCT ENSP00000499139.1:n.885-95_885-94insTCT
ENST00000295497.11:c.834-95_834-94insTCT ENSP00000295497.7:n.834-95_834-94insTCT
ENST00000409156.7:c.1131-95_1131-94insTCT ENSP00000386470.3:n.1131-95_1131-94insTCT
ENST00000409597.5:c.657-95_657-94insTCT ENSP00000386469.1:n.657-95_657-94insTCT
ENST00000409900.7:c.1209-95_1209-94insTCT ENSP00000386741.3:n.1209-95_1209-94insTCT
ENST00000488080.5:n.1060-95_1060-94insTCT
ENST00000492964.1:n.352-95_352-94insTCT
NM_001025201.3:c.1131-95_1131-94insTCT NP_001020372.2:n.1131-95_1131-94insTCT
NM_001206602.1:c.834-95_834-94insTCT NP_001193531.1:n.834-95_834-94insTCT
NM_001822.5:c.1209-95_1209-94insTCT NP_001813.1:n.1209-95_1209-94insTCT
NR_038133.1:n.1075-95_1075-94insTCT
NM_001025201.4:c.1131-95_1131-94insTCT NP_001020372.2:n.1131-95_1131-94insTCT
NM_001206602.2:c.834-95_834-94insTCT NP_001193531.1:n.834-95_834-94insTCT
NM_001371513.1:c.1209-95_1209-94insTCT NP_001358442.1:n.1209-95_1209-94insTCT
NM_001371514.1:c.1260-95_1260-94insTCT NP_001358443.1:n.1260-95_1260-94insTCT
NM_001822.7:c.1209-95_1209-94insTCT MANE Select NP_001813.1:n.1209-95_1209-94insTCT
NR_038133.2:n.1077-95_1077-94insTCT