Canonical Allele Identifier: CA961672
Gene: CNN3 HGNC NCBI
CNN3-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94926849C>T , CM000663.2:g.94926849C>T GRCh38
NC_000001.10:g.95392405C>T , CM000663.1:g.95392405C>T GRCh37
NC_000001.9:g.95164993C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370206.9:c.46G>A (CNN3) MANE Select ENSP00000359225.4:p.Val16Ile
ENST00000370206.8:c.46G>A (CNN3) ENSP00000359225.4:p.Val16Ile
ENST00000394202.8:c.46G>A (CNN3) ENSP00000377752.4:p.Val16Ile
NM_001286055.1:c.46G>A (CNN3) NP_001272984.1:p.Val16Ile
NM_001839.4:c.46G>A (CNN3) NP_001830.1:p.Val16Ile
XM_011542527.1:c.329+109C>T XP_011540829.1:n.329+109C>T
XM_011542527.2:c.329+109C>T XP_011540829.1:n.329+109C>T
NM_001839.5:c.46G>A (CNN3) MANE Select NP_001830.1:p.Val16Ile
NM_001286055.2:c.46G>A (CNN3) NP_001272984.1:p.Val16Ile
NR_168376.1:n.381+109C>T (CNN3-DT)
NR_168377.1:n.381+109C>T (CNN3-DT)