Canonical Allele Identifier: CA1308865696
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174824461G= , CM000664.2:g.174824461G= GRCh38
NC_000002.11:g.175689189G= , CM000664.1:g.175689189G= GRCh37
NC_000002.10:g.175397435G= NCBI36
NG_012642.1:g.185982C=
NG_012642.2:g.185982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.310C= ENSP00000295497.7:p.Leu104=
ENST00000444394.7:c.310C= ENSP00000411911.2:p.Leu104=
ENST00000295497.12:c.310C= ENSP00000295497.7:p.Leu104=
ENST00000409089.7:c.10C= ENSP00000386322.3:p.Leu4=
ENST00000409900.9:c.685C= MANE Select ENSP00000386741.4:p.Leu229=
ENST00000413882.6:c.139C= ENSP00000410496.2:p.Leu47=
ENST00000425395.6:c.*132C= ENSP00000405270.2:n.*132C=
ENST00000443238.6:c.163C= ENSP00000409798.2:p.Leu55=
ENST00000444394.6:c.310C= ENSP00000411911.2:p.Leu104=
ENST00000444573.2:c.529C= ENSP00000392603.2:p.Leu177=
ENST00000488080.6:n.328C=
ENST00000650731.1:c.10C= ENSP00000499146.1:p.Leu4=
ENST00000650938.1:c.209C=
ENST00000651246.1:c.277C= ENSP00000498484.1:p.Leu93=
ENST00000651373.1:c.199C= ENSP00000499174.1:p.Leu67=
ENST00000651501.1:c.*132C= ENSP00000498894.1:n.*132C=
ENST00000651717.1:c.253-11979C= ENSP00000499124.1:n.253-11979C=
ENST00000652036.1:c.310C= ENSP00000499139.1:p.Leu104=
ENST00000652154.1:n.583C=
ENST00000295497.11:c.310C= ENSP00000295497.7:p.Leu104=
ENST00000409089.6:c.10C= ENSP00000386322.2:p.Leu4=
ENST00000409156.7:c.607C= ENSP00000386470.3:p.Leu203=
ENST00000409597.5:c.133C= ENSP00000386469.1:p.Leu45=
ENST00000409900.7:c.685C= ENSP00000386741.3:p.Leu229=
ENST00000413882.5:c.139C= ENSP00000410496.1:p.Leu47=
ENST00000425395.5:c.*236C= ENSP00000405270.1:n.*236C=
ENST00000443238.5:c.163C= ENSP00000409798.1:p.Leu55=
ENST00000444394.5:c.10C= ENSP00000411911.1:p.Leu4=
ENST00000444573.1:c.310C= ENSP00000392603.1:p.Leu104=
ENST00000485882.1:n.144C=
ENST00000488080.5:n.536C=
NM_001025201.3:c.607C= NP_001020372.2:p.Leu203=
NM_001206602.1:c.310C= NP_001193531.1:p.Leu104=
NM_001822.5:c.685C= NP_001813.1:p.Leu229=
NR_038133.1:n.551C=
NM_001025201.4:c.607C= NP_001020372.2:p.Leu203=
NM_001206602.2:c.310C= NP_001193531.1:p.Leu104=
NM_001371513.1:c.685C= NP_001358442.1:p.Leu229=
NM_001371514.1:c.736C= NP_001358443.1:p.Leu246=
NM_001822.7:c.685C= MANE Select NP_001813.1:p.Leu229=
NR_038133.2:n.553C=