Canonical Allele Identifier: CA802073225

Gene: CTNND2

Linked Data

• dbSNP Id: rs1157163281
• gnomAD v3: 5-11320438-A-G
• gnomAD v4: 5-11320438-A-G
• MyVariant Identifiers: chr5:g.11320550A>G (hg19) ; chr5:g.11320438A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11320438A>G , CM000667.2:g.11320438A>G	GRCh38
NC_000005.9:g.11320550A>G , CM000667.1:g.11320550A>G	GRCh37
NC_000005.8:g.11373550A>G	NCBI36
NG_023544.1:g.588561T>C
NG_023544.2:g.588561T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706271.1:c.617+25934T>C	ENSP00000516315.1:n.617+25934T>C
ENST00000706272.1:c.700+25934T>C
ENST00000304623.13:c.1628+25934T>C MANE Select	ENSP00000307134.8:n.1628+25934T>C
ENST00000304623.12:c.1628+25934T>C	ENSP00000307134.8:n.1628+25934T>C
ENST00000495388.6:n.713+25934T>C
ENST00000503622.5:c.617+25934T>C	ENSP00000426887.1:n.617+25934T>C
ENST00000504499.5:c.*367+25934T>C	ENSP00000421000.1:n.*367+25934T>C
ENST00000511377.5:c.1355+25934T>C	ENSP00000426510.1:n.1355+25934T>C
ENST00000513588.5:c.890+25934T>C	ENSP00000421093.1:n.890+25934T>C
NM_001288715.1:c.1355+25934T>C	NP_001275644.1:n.1355+25934T>C
NM_001288716.1:c.617+25934T>C	NP_001275645.1:n.617+25934T>C
NM_001288717.1:c.329+25934T>C	NP_001275646.1:n.329+25934T>C
NM_001332.3:c.1628+25934T>C	NP_001323.1:n.1628+25934T>C
NR_109988.1:n.1080+25934T>C
XM_005248251.2:c.1628+25934T>C	XP_005248308.1:n.1628+25934T>C
XM_005248252.1:c.1586+25934T>C	XP_005248309.1:n.1586+25934T>C
XM_005248253.1:c.1355+25934T>C	XP_005248310.1:n.1355+25934T>C
XM_011513967.1:c.1355+25934T>C	XP_011512269.1:n.1355+25934T>C
NM_001364128.1:c.617+25934T>C	NP_001351057.1:n.617+25934T>C
XM_005248251.3:c.1628+25934T>C	XP_005248308.1:n.1628+25934T>C
XM_005248252.2:c.1586+25934T>C	XP_005248309.1:n.1586+25934T>C
XM_011513967.2:c.1355+25934T>C	XP_011512269.1:n.1355+25934T>C
XM_017009072.1:c.890+25934T>C	XP_016864561.1:n.890+25934T>C
XM_017009073.1:c.848+25934T>C	XP_016864562.1:n.848+25934T>C
XM_017009074.1:c.890+25934T>C	XP_016864563.1:n.890+25934T>C
XM_017009075.2:c.617+25934T>C	XP_016864564.1:n.617+25934T>C
XM_024454368.1:c.-44+44258T>C	XP_024310136.1:n.-44+44258T>C
NM_001332.4:c.1628+25934T>C MANE Select	NP_001323.1:n.1628+25934T>C
NM_001288717.2:c.329+25934T>C	NP_001275646.1:n.329+25934T>C
NR_109988.2:n.1483+25934T>C
NM_001364128.2:c.617+25934T>C	NP_001351057.1:n.617+25934T>C