Canonical Allele Identifier: CA1308889409
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174877913T= , CM000664.2:g.174877913T= GRCh38
NC_000002.11:g.175742641T= , CM000664.1:g.175742641T= GRCh37
NC_000002.10:g.175450887T= NCBI36
NG_012642.1:g.132530A=
NG_012642.2:g.132530A=

Transcript Alleles

HGVS Amino-acid change
ENST00000409900.9:c.476A= MANE Select ENSP00000386741.4:p.Lys159=
ENST00000425395.6:c.105-30956A= ENSP00000405270.2:n.105-30956A=
ENST00000444573.2:c.320A= ENSP00000392603.2:p.Lys107=
ENST00000451799.2:c.320A= ENSP00000416316.2:p.Lys107=
ENST00000469597.2:c.*124A= ENSP00000498417.1:n.*124A=
ENST00000488080.6:n.115-2048A=
ENST00000650734.1:c.*376A= ENSP00000498742.1:n.*376A=
ENST00000650770.1:c.*390A= ENSP00000499036.1:n.*390A=
ENST00000651063.1:n.527A=
ENST00000651246.1:c.68A= ENSP00000498484.1:p.Lys23=
ENST00000651315.1:c.68A= ENSP00000498692.1:p.Lys23=
ENST00000651373.1:c.68A= ENSP00000499174.1:p.Lys23=
ENST00000651501.1:c.105-30956A= ENSP00000498894.1:n.105-30956A=
ENST00000651580.1:c.320A= ENSP00000498631.1:p.Lys107=
ENST00000651599.1:c.320A= ENSP00000498535.1:p.Lys107=
ENST00000651803.1:c.*390A= ENSP00000499007.1:n.*390A=
ENST00000651971.1:c.*276A= ENSP00000499035.1:n.*276A=
ENST00000652154.1:n.452A=
ENST00000652208.1:c.320A= ENSP00000498475.1:p.Lys107=
ENST00000652434.1:c.437A= ENSP00000498549.1:p.Lys146=
ENST00000652437.1:n.619A=
ENST00000652674.1:c.68A= ENSP00000498599.1:p.Lys23=
ENST00000652734.1:n.373A=
ENST00000652756.1:c.320A= ENSP00000498281.1:p.Lys107=
ENST00000652768.1:n.368A=
ENST00000409156.7:c.476A= ENSP00000386470.3:p.Lys159=
ENST00000409900.7:c.476A= ENSP00000386741.3:p.Lys159=
ENST00000425395.5:c.*101-30956A= ENSP00000405270.1:n.*101-30956A=
ENST00000469597.1:n.581A=
ENST00000481174.1:n.29A=
ENST00000488080.5:n.401-30956A=
ENST00000490654.1:n.451A=
NM_001025201.3:c.476A= NP_001020372.2:p.Lys159=
NM_001822.5:c.476A= NP_001813.1:p.Lys159=
NR_038133.1:n.416-30956A=
NM_001025201.4:c.476A= NP_001020372.2:p.Lys159=
NM_001371513.1:c.476A= NP_001358442.1:p.Lys159=
NM_001371514.1:c.527A= NP_001358443.1:p.Lys176=
NM_001822.7:c.476A= MANE Select NP_001813.1:p.Lys159=
NR_038133.2:n.418-30956A=