Canonical Allele Identifier: CA9032070

Gene: CNN2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1036232G>A , CM000681.2:g.1036232G>A	GRCh38
NC_000019.9:g.1036231G>A , CM000681.1:g.1036231G>A	GRCh37
NC_000019.8:g.987231G>A	NCBI36
NG_046909.1:g.1130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263097.9:c.493G>A MANE Select	ENSP00000263097.2:p.Val165Ile
ENST00000568865.3:c.493G>A	ENSP00000458137.2:p.Val165Ile
ENST00000263097.8:c.493G>A	ENSP00000263097.2:p.Val165Ile
ENST00000348419.7:c.391-184G>A	ENSP00000340129.2:n.391-184G>A
ENST00000562075.6:c.202-184G>A	ENSP00000455777.2:n.202-184G>A
ENST00000562958.6:c.556G>A	ENSP00000456436.1:p.Val186Ile
ENST00000565096.6:c.460G>A	ENSP00000457968.1:p.Val154Ile
ENST00000566695.5:c.304G>A	ENSP00000484533.1:p.Val102Ile
ENST00000568865.2:c.364G>A	ENSP00000458137.1:p.Val122Ile
ENST00000569352.6:c.*169-1318G>A	ENSP00000468577.1:n.*169-1318G>A
ENST00000606983.5:c.466G>A	ENSP00000484749.1:p.Val156Ile
ENST00000607102.1:c.35-184G>A
NM_001303499.1:c.460G>A	NP_001290428.1:p.Val154Ile
NM_001303501.1:c.556G>A	NP_001290430.1:p.Val186Ile
NM_004368.3:c.493G>A	NP_004359.1:p.Val165Ile
NM_201277.2:c.391-184G>A	NP_958434.1:n.391-184G>A
NM_004368.4:c.493G>A MANE Select	NP_004359.1:p.Val165Ile
NM_001303499.2:c.460G>A	NP_001290428.1:p.Val154Ile
NM_001303501.2:c.556G>A	NP_001290430.1:p.Val186Ile
NM_201277.3:c.391-184G>A	NP_958434.1:n.391-184G>A