Canonical Allele Identifier: CA1308865712
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824513A= , CM000664.2:g.174824513A= GRCh38
NC_000002.11:g.175689241A= , CM000664.1:g.175689241A= GRCh37
NC_000002.10:g.175397487A= NCBI36
NG_012642.1:g.185930T=
NG_012642.2:g.185930T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.258T= ENSP00000295497.7:p.His86=
ENST00000444394.7:c.258T= ENSP00000411911.2:p.His86=
ENST00000295497.12:c.258T= ENSP00000295497.7:p.His86=
ENST00000409089.7:c.-43T= ENSP00000386322.3:n.-43T=
ENST00000409900.9:c.633T= MANE Select ENSP00000386741.4:p.His211=
ENST00000413882.6:c.87T= ENSP00000410496.2:p.His29=
ENST00000425395.6:c.*80T= ENSP00000405270.2:n.*80T=
ENST00000443238.6:c.111T= ENSP00000409798.2:p.His37=
ENST00000444394.6:c.258T= ENSP00000411911.2:p.His86=
ENST00000444573.2:c.477T= ENSP00000392603.2:p.His159=
ENST00000451799.2:c.477T= ENSP00000416316.2:p.His159=
ENST00000469597.2:c.*281T= ENSP00000498417.1:n.*281T=
ENST00000488080.6:n.276T=
ENST00000650731.1:c.-43T= ENSP00000499146.1:n.-43T=
ENST00000650734.1:c.*533T= ENSP00000498742.1:n.*533T=
ENST00000650770.1:c.*547T= ENSP00000499036.1:n.*547T=
ENST00000650938.1:c.157T=
ENST00000651246.1:c.225T= ENSP00000498484.1:p.His75=
ENST00000651315.1:c.225T= ENSP00000498692.1:p.His75=
ENST00000651373.1:c.147T= ENSP00000499174.1:p.His49=
ENST00000651501.1:c.*80T= ENSP00000498894.1:n.*80T=
ENST00000651580.1:c.*212T= ENSP00000498631.1:n.*212T=
ENST00000651599.1:c.*117T= ENSP00000498535.1:n.*117T=
ENST00000651717.1:c.253-12031T= ENSP00000499124.1:n.253-12031T=
ENST00000651803.1:c.*625T= ENSP00000499007.1:n.*625T=
ENST00000651971.1:c.*433T= ENSP00000499035.1:n.*433T=
ENST00000652036.1:c.258T= ENSP00000499139.1:p.His86=
ENST00000652154.1:n.531T=
ENST00000652208.1:c.477T= ENSP00000498475.1:p.His159=
ENST00000652434.1:c.594T= ENSP00000498549.1:p.His198=
ENST00000652437.1:n.776T=
ENST00000652674.1:c.*117T= ENSP00000498599.1:n.*117T=
ENST00000652734.1:n.530T=
ENST00000652756.1:c.477T= ENSP00000498281.1:p.His159=
ENST00000652768.1:n.525T=
ENST00000295497.11:c.258T= ENSP00000295497.7:p.His86=
ENST00000409089.6:c.-43T= ENSP00000386322.2:n.-43T=
ENST00000409156.7:c.555T= ENSP00000386470.3:p.His185=
ENST00000409597.5:c.81T= ENSP00000386469.1:p.His27=
ENST00000409900.7:c.633T= ENSP00000386741.3:p.His211=
ENST00000413882.5:c.87T= ENSP00000410496.1:p.His29=
ENST00000425395.5:c.*184T= ENSP00000405270.1:n.*184T=
ENST00000443238.5:c.111T= ENSP00000409798.1:p.His37=
ENST00000444394.5:c.-43T= ENSP00000411911.1:n.-43T=
ENST00000444573.1:c.258T= ENSP00000392603.1:p.His86=
ENST00000485882.1:n.92T=
ENST00000488080.5:n.484T=
NM_001025201.3:c.555T= NP_001020372.2:p.His185=
NM_001206602.1:c.258T= NP_001193531.1:p.His86=
NM_001822.5:c.633T= NP_001813.1:p.His211=
NR_038133.1:n.499T=
NM_001025201.4:c.555T= NP_001020372.2:p.His185=
NM_001206602.2:c.258T= NP_001193531.1:p.His86=
NM_001371513.1:c.633T= NP_001358442.1:p.His211=
NM_001371514.1:c.684T= NP_001358443.1:p.His228=
NM_001822.7:c.633T= MANE Select NP_001813.1:p.His211=
NR_038133.2:n.501T=