Canonical Allele Identifier: CA359281388

Gene: CTNND2

Linked Data

• MyVariant Identifiers: chr5:g.11384998A>T (hg19) ; chr5:g.11384886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11384886A>T , CM000667.2:g.11384886A>T	GRCh38
NC_000005.9:g.11384998A>T , CM000667.1:g.11384998A>T	GRCh37
NC_000005.8:g.11437998A>T	NCBI36
NG_023544.1:g.524113T>A
NG_023544.2:g.524113T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-19996T>A	ENSP00000516315.1:n.167-19996T>A
ENST00000706272.1:c.28T>A
ENST00000304623.13:c.956T>A MANE Select	ENSP00000307134.8:p.Ile319Asn
ENST00000304623.12:c.956T>A	ENSP00000307134.8:p.Ile319Asn
ENST00000502551.5:c.398-19996T>A	ENSP00000422389.1:n.398-19996T>A
ENST00000503622.5:c.167-19996T>A	ENSP00000426887.1:n.167-19996T>A
ENST00000504354.5:n.217-19996T>A
ENST00000504499.5:c.612+12145T>A	ENSP00000421000.1:n.612+12145T>A
ENST00000506735.1:n.27T>A
ENST00000507430.1:n.52T>A
ENST00000511278.5:n.542-19996T>A
ENST00000511377.5:c.683T>A	ENSP00000426510.1:p.Ile228Asn
ENST00000513588.5:c.440-19996T>A	ENSP00000421093.1:n.440-19996T>A
NM_001288715.1:c.683T>A	NP_001275644.1:p.Ile228Asn
NM_001288716.1:c.167-19996T>A	NP_001275645.1:n.167-19996T>A
NM_001288717.1:c.-123+12145T>A	NP_001275646.1:n.-123+12145T>A
NM_001332.3:c.956T>A	NP_001323.1:p.Ile319Asn
NR_109988.1:n.630-19996T>A
XM_005248251.2:c.956T>A	XP_005248308.1:p.Ile319Asn
XM_005248252.1:c.914T>A	XP_005248309.1:p.Ile305Asn
XM_005248253.1:c.683T>A	XP_005248310.1:p.Ile228Asn
XM_011513967.1:c.683T>A	XP_011512269.1:p.Ile228Asn
NM_001364128.1:c.167-19996T>A	NP_001351057.1:n.167-19996T>A
XM_005248251.3:c.956T>A	XP_005248308.1:p.Ile319Asn
XM_005248252.2:c.914T>A	XP_005248309.1:p.Ile305Asn
XM_011513967.2:c.683T>A	XP_011512269.1:p.Ile228Asn
XM_017009072.1:c.440-19996T>A	XP_016864561.1:n.440-19996T>A
XM_017009073.1:c.398-19996T>A	XP_016864562.1:n.398-19996T>A
XM_017009074.1:c.440-19996T>A	XP_016864563.1:n.440-19996T>A
XM_017009075.2:c.167-19996T>A	XP_016864564.1:n.167-19996T>A
XM_024454368.1:c.-460T>A	XP_024310136.1:n.-460T>A
NM_001332.4:c.956T>A MANE Select	NP_001323.1:p.Ile319Asn
NM_001288717.2:c.-123+12145T>A	NP_001275646.1:n.-123+12145T>A
NR_109988.2:n.1033-19996T>A
NM_001364128.2:c.167-19996T>A	NP_001351057.1:n.167-19996T>A