Canonical Allele Identifier: CA341362190

Gene: CNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94897929T>C , CM000663.2:g.94897929T>C	GRCh38
NC_000001.10:g.95363485T>C , CM000663.1:g.95363485T>C	GRCh37
NC_000001.9:g.95136073T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370206.9:c.803A>G MANE Select	ENSP00000359225.4:p.Tyr268Cys
ENST00000370206.8:c.803A>G	ENSP00000359225.4:p.Tyr268Cys
ENST00000394202.8:c.665A>G	ENSP00000377752.4:p.Tyr222Cys
ENST00000461018.5:n.507A>G
ENST00000545882.5:c.680A>G	ENSP00000440081.1:p.Tyr227Cys
NM_001286055.1:c.665A>G	NP_001272984.1:p.Tyr222Cys
NM_001286056.1:c.680A>G	NP_001272985.1:p.Tyr227Cys
NM_001839.4:c.803A>G	NP_001830.1:p.Tyr268Cys
XM_017000245.2:c.680A>G	XP_016855734.1:p.Tyr227Cys
NM_001839.5:c.803A>G MANE Select	NP_001830.1:p.Tyr268Cys
NM_001286055.2:c.665A>G	NP_001272984.1:p.Tyr222Cys
NM_001286056.2:c.680A>G	NP_001272985.1:p.Tyr227Cys