Canonical Allele Identifier: CA341361834

Gene: CNN3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94897774A>G , CM000663.2:g.94897774A>G	GRCh38
NC_000001.10:g.95363330A>G , CM000663.1:g.95363330A>G	GRCh37
NC_000001.9:g.95135918A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370206.9:c.958T>C MANE Select	ENSP00000359225.4:p.Tyr320His
ENST00000370206.8:c.958T>C	ENSP00000359225.4:p.Tyr320His
ENST00000394202.8:c.820T>C	ENSP00000377752.4:p.Tyr274His
ENST00000545882.5:c.835T>C	ENSP00000440081.1:p.Tyr279His
NM_001286055.1:c.820T>C	NP_001272984.1:p.Tyr274His
NM_001286056.1:c.835T>C	NP_001272985.1:p.Tyr279His
NM_001839.4:c.958T>C	NP_001830.1:p.Tyr320His
XM_017000245.2:c.835T>C	XP_016855734.1:p.Tyr279His
NM_001839.5:c.958T>C MANE Select	NP_001830.1:p.Tyr320His
NM_001286055.2:c.820T>C	NP_001272984.1:p.Tyr274His
NM_001286056.2:c.835T>C	NP_001272985.1:p.Tyr279His