Canonical Allele Identifier: CA1308854820
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800004G= , CM000664.2:g.174800004G= GRCh38
NC_000002.11:g.175664732G= , CM000664.1:g.175664732G= GRCh37
NC_000002.10:g.175372978G= NCBI36
NG_012642.1:g.210439C=
NG_012642.2:g.210439C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295497.13:c.*112C= ENSP00000295497.7:n.*112C=
ENST00000295497.12:c.*112C= ENSP00000295497.7:n.*112C=
ENST00000409900.9:c.*112C= MANE Select ENSP00000386741.4:n.*112C=
ENST00000413882.6:c.*112C= ENSP00000410496.2:n.*112C=
ENST00000443238.6:c.*112C= ENSP00000409798.2:n.*112C=
ENST00000488080.6:n.1135C=
ENST00000650731.1:c.*112C= ENSP00000499146.1:n.*112C=
ENST00000650938.1:c.878C=
ENST00000651246.1:c.*112C= ENSP00000498484.1:n.*112C=
ENST00000651501.1:c.*939C= ENSP00000498894.1:n.*939C=
ENST00000651717.1:c.*768C= ENSP00000499124.1:n.*768C=
ENST00000652036.1:c.*112C= ENSP00000499139.1:n.*112C=
ENST00000295497.11:c.*112C= ENSP00000295497.7:n.*112C=
ENST00000409156.7:c.*112C= ENSP00000386470.3:n.*112C=
ENST00000409597.5:c.*112C= ENSP00000386469.1:n.*112C=
ENST00000409900.7:c.*112C= ENSP00000386741.3:n.*112C=
ENST00000488080.5:n.1343C=
ENST00000492964.1:n.635C=
NM_001025201.3:c.*112C= NP_001020372.2:n.*112C=
NM_001206602.1:c.*112C= NP_001193531.1:n.*112C=
NM_001822.5:c.*112C= NP_001813.1:n.*112C=
NR_038133.1:n.1358C=
NM_001025201.4:c.*112C= NP_001020372.2:n.*112C=
NM_001206602.2:c.*112C= NP_001193531.1:n.*112C=
NM_001371513.1:c.*112C= NP_001358442.1:n.*112C=
NM_001371514.1:c.*112C= NP_001358443.1:n.*112C=
NM_001822.7:c.*112C= MANE Select NP_001813.1:n.*112C=
NR_038133.2:n.1360C=