Canonical Allele Identifier: CA430300613

Gene: CHN1

Linked Data

• gnomAD v4: 2-174878029-G-T
• MyVariant Identifiers: chr2:g.175742757G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174878029G>T , CM000664.2:g.174878029G>T	GRCh38
NC_000002.11:g.175742757G>T , CM000664.1:g.175742757G>T	GRCh37
NC_000002.10:g.175451003G>T	NCBI36
NG_012642.1:g.132414C>A
NG_012642.2:g.132414C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409900.9:c.360C>A MANE Select	ENSP00000386741.4:p.Gly120=
ENST00000425395.6:c.105-31072C>A	ENSP00000405270.2:n.105-31072C>A
ENST00000444573.2:c.204C>A	ENSP00000392603.2:p.Gly68=
ENST00000451799.2:c.204C>A	ENSP00000416316.2:p.Gly68=
ENST00000469597.2:c.*8C>A	ENSP00000498417.1:n.*8C>A
ENST00000488080.6:n.115-2164C>A
ENST00000650734.1:c.*260C>A	ENSP00000498742.1:n.*260C>A
ENST00000650770.1:c.*274C>A	ENSP00000499036.1:n.*274C>A
ENST00000651063.1:n.411C>A
ENST00000651246.1:c.-49C>A	ENSP00000498484.1:n.-49C>A
ENST00000651315.1:c.-49C>A	ENSP00000498692.1:n.-49C>A
ENST00000651373.1:c.-49C>A	ENSP00000499174.1:n.-49C>A
ENST00000651501.1:c.105-31072C>A	ENSP00000498894.1:n.105-31072C>A
ENST00000651580.1:c.204C>A	ENSP00000498631.1:p.Gly68=
ENST00000651599.1:c.204C>A	ENSP00000498535.1:p.Gly68=
ENST00000651803.1:c.*274C>A	ENSP00000499007.1:n.*274C>A
ENST00000651971.1:c.*160C>A	ENSP00000499035.1:n.*160C>A
ENST00000652154.1:n.336C>A
ENST00000652208.1:c.204C>A	ENSP00000498475.1:p.Gly68=
ENST00000652434.1:c.321C>A	ENSP00000498549.1:p.Gly107=
ENST00000652437.1:n.503C>A
ENST00000652674.1:c.-49C>A	ENSP00000498599.1:n.-49C>A
ENST00000652734.1:n.257C>A
ENST00000652756.1:c.204C>A	ENSP00000498281.1:p.Gly68=
ENST00000652768.1:n.252C>A
ENST00000409156.7:c.360C>A	ENSP00000386470.3:p.Gly120=
ENST00000409900.7:c.360C>A	ENSP00000386741.3:p.Gly120=
ENST00000425395.5:c.*101-31072C>A	ENSP00000405270.1:n.*101-31072C>A
ENST00000469597.1:n.465C>A
ENST00000488080.5:n.401-31072C>A
ENST00000490654.1:n.335C>A
NM_001025201.3:c.360C>A	NP_001020372.2:p.Gly120=
NM_001822.5:c.360C>A	NP_001813.1:p.Gly120=
NR_038133.1:n.416-31072C>A
NM_001025201.4:c.360C>A	NP_001020372.2:p.Gly120=
NM_001371513.1:c.360C>A	NP_001358442.1:p.Gly120=
NM_001371514.1:c.411C>A	NP_001358443.1:p.Gly137=
NM_001822.7:c.360C>A MANE Select	NP_001813.1:p.Gly120=
NR_038133.2:n.418-31072C>A