Canonical Allele Identifier: CA1308865699
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824474G= , CM000664.2:g.174824474G= GRCh38
NC_000002.11:g.175689202G= , CM000664.1:g.175689202G= GRCh37
NC_000002.10:g.175397448G= NCBI36
NG_012642.1:g.185969C=
NG_012642.2:g.185969C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.297C= ENSP00000295497.7:p.Asn99=
ENST00000444394.7:c.297C= ENSP00000411911.2:p.Asn99=
ENST00000295497.12:c.297C= ENSP00000295497.7:p.Asn99=
ENST00000409089.7:c.-4C= ENSP00000386322.3:n.-4C=
ENST00000409900.9:c.672C= MANE Select ENSP00000386741.4:p.Asn224=
ENST00000413882.6:c.126C= ENSP00000410496.2:p.Asn42=
ENST00000425395.6:c.*119C= ENSP00000405270.2:n.*119C=
ENST00000443238.6:c.150C= ENSP00000409798.2:p.Asn50=
ENST00000444394.6:c.297C= ENSP00000411911.2:p.Asn99=
ENST00000444573.2:c.516C= ENSP00000392603.2:p.Asn172=
ENST00000488080.6:n.315C=
ENST00000650731.1:c.-4C= ENSP00000499146.1:n.-4C=
ENST00000650938.1:c.196C=
ENST00000651246.1:c.264C= ENSP00000498484.1:p.Asn88=
ENST00000651373.1:c.186C= ENSP00000499174.1:p.Asn62=
ENST00000651501.1:c.*119C= ENSP00000498894.1:n.*119C=
ENST00000651717.1:c.253-11992C= ENSP00000499124.1:n.253-11992C=
ENST00000652036.1:c.297C= ENSP00000499139.1:p.Asn99=
ENST00000652154.1:n.570C=
ENST00000295497.11:c.297C= ENSP00000295497.7:p.Asn99=
ENST00000409089.6:c.-4C= ENSP00000386322.2:n.-4C=
ENST00000409156.7:c.594C= ENSP00000386470.3:p.Asn198=
ENST00000409597.5:c.120C= ENSP00000386469.1:p.Asn40=
ENST00000409900.7:c.672C= ENSP00000386741.3:p.Asn224=
ENST00000413882.5:c.126C= ENSP00000410496.1:p.Asn42=
ENST00000425395.5:c.*223C= ENSP00000405270.1:n.*223C=
ENST00000443238.5:c.150C= ENSP00000409798.1:p.Asn50=
ENST00000444394.5:c.-4C= ENSP00000411911.1:n.-4C=
ENST00000444573.1:c.297C= ENSP00000392603.1:p.Asn99=
ENST00000485882.1:n.131C=
ENST00000488080.5:n.523C=
NM_001025201.3:c.594C= NP_001020372.2:p.Asn198=
NM_001206602.1:c.297C= NP_001193531.1:p.Asn99=
NM_001822.5:c.672C= NP_001813.1:p.Asn224=
NR_038133.1:n.538C=
NM_001025201.4:c.594C= NP_001020372.2:p.Asn198=
NM_001206602.2:c.297C= NP_001193531.1:p.Asn99=
NM_001371513.1:c.672C= NP_001358442.1:p.Asn224=
NM_001371514.1:c.723C= NP_001358443.1:p.Asn241=
NM_001822.7:c.672C= MANE Select NP_001813.1:p.Asn224=
NR_038133.2:n.540C=