Canonical Allele Identifier: CA359278822

Gene: CTNND2

Linked Data

• MyVariant Identifiers: chr5:g.11346685T>A (hg19) ; chr5:g.11346573T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346573T>A , CM000667.2:g.11346573T>A	GRCh38
NC_000005.9:g.11346685T>A , CM000667.1:g.11346685T>A	GRCh37
NC_000005.8:g.11399685T>A	NCBI36
NG_023544.1:g.562426A>T
NG_023544.2:g.562426A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.416A>T	ENSP00000516315.1:p.His139Leu
ENST00000706272.1:c.499A>T
ENST00000304623.13:c.1427A>T MANE Select	ENSP00000307134.8:p.His476Leu
ENST00000304623.12:c.1427A>T	ENSP00000307134.8:p.His476Leu
ENST00000495388.6:n.512A>T
ENST00000503622.5:c.416A>T	ENSP00000426887.1:p.His139Leu
ENST00000504354.5:n.466A>T
ENST00000504499.5:c.*166A>T	ENSP00000421000.1:n.*166A>T
ENST00000511377.5:c.1154A>T	ENSP00000426510.1:p.His385Leu
ENST00000513588.5:c.689A>T	ENSP00000421093.1:p.His230Leu
NM_001288715.1:c.1154A>T	NP_001275644.1:p.His385Leu
NM_001288716.1:c.416A>T	NP_001275645.1:p.His139Leu
NM_001288717.1:c.128A>T	NP_001275646.1:p.His43Leu
NM_001332.3:c.1427A>T	NP_001323.1:p.His476Leu
NR_109988.1:n.879A>T
XM_005248251.2:c.1427A>T	XP_005248308.1:p.His476Leu
XM_005248252.1:c.1385A>T	XP_005248309.1:p.His462Leu
XM_005248253.1:c.1154A>T	XP_005248310.1:p.His385Leu
XM_011513967.1:c.1154A>T	XP_011512269.1:p.His385Leu
NM_001364128.1:c.416A>T	NP_001351057.1:p.His139Leu
XM_005248251.3:c.1427A>T	XP_005248308.1:p.His476Leu
XM_005248252.2:c.1385A>T	XP_005248309.1:p.His462Leu
XM_011513967.2:c.1154A>T	XP_011512269.1:p.His385Leu
XM_017009072.1:c.689A>T	XP_016864561.1:p.His230Leu
XM_017009073.1:c.647A>T	XP_016864562.1:p.His216Leu
XM_017009074.1:c.689A>T	XP_016864563.1:p.His230Leu
XM_017009075.2:c.416A>T	XP_016864564.1:p.His139Leu
XM_024454368.1:c.-44+18123A>T	XP_024310136.1:n.-44+18123A>T
NM_001332.4:c.1427A>T MANE Select	NP_001323.1:p.His476Leu
NM_001288717.2:c.128A>T	NP_001275646.1:p.His43Leu
NR_109988.2:n.1282A>T
NM_001364128.2:c.416A>T	NP_001351057.1:p.His139Leu