Canonical Allele Identifier: CA9032065

Gene: CNN2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1036202G>A , CM000681.2:g.1036202G>A	GRCh38
NC_000019.9:g.1036201G>A , CM000681.1:g.1036201G>A	GRCh37
NC_000019.8:g.987201G>A	NCBI36
NG_046909.1:g.1100G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004368.4:c.463G>A MANE Select	NP_004359.1:p.Asp155Asn
ENST00000263097.9:c.463G>A MANE Select	ENSP00000263097.2:p.Asp155Asn
NM_001303499.1:c.430G>A	NP_001290428.1:p.Asp144Asn
NM_001303499.2:c.430G>A	NP_001290428.1:p.Asp144Asn
NM_001303501.1:c.526G>A	NP_001290430.1:p.Asp176Asn
NM_001303501.2:c.526G>A	NP_001290430.1:p.Asp176Asn
NM_004368.3:c.463G>A	NP_004359.1:p.Asp155Asn
NM_201277.2:c.391-214G>A	NP_958434.1:n.391-214G>A
NM_201277.3:c.391-214G>A	NP_958434.1:n.391-214G>A
ENST00000263097.8:c.463G>A	ENSP00000263097.2:p.Asp155Asn
ENST00000348419.7:c.391-214G>A	ENSP00000340129.2:n.391-214G>A
ENST00000562075.6:c.202-214G>A	ENSP00000455777.2:n.202-214G>A
ENST00000562958.6:c.526G>A	ENSP00000456436.1:p.Asp176Asn
ENST00000565096.6:c.430G>A	ENSP00000457968.1:p.Asp144Asn
ENST00000566695.5:c.274G>A	ENSP00000484533.1:p.Asp92Asn
ENST00000568865.2:c.334G>A	ENSP00000458137.1:p.Asp112Asn
ENST00000568865.3:c.463G>A	ENSP00000458137.2:p.Asp155Asn
ENST00000569352.6:c.*169-1348G>A	ENSP00000468577.1:n.*169-1348G>A
ENST00000606983.5:c.436G>A	ENSP00000484749.1:p.Asp146Asn
ENST00000607102.1:c.35-214G>A