Canonical Allele Identifier: CA443541246

Gene: CTNND2

Linked Data

• dbSNP Id: rs1380302730
• gnomAD v2: 5-11346636-G-A
• gnomAD v4: 5-11346524-G-A
• MyVariant Identifiers: chr5:g.11346636G>A (hg19) ; chr5:g.11346524G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346524G>A , CM000667.2:g.11346524G>A	GRCh38
NC_000005.9:g.11346636G>A , CM000667.1:g.11346636G>A	GRCh37
NC_000005.8:g.11399636G>A	NCBI36
NG_023544.1:g.562475C>T
NG_023544.2:g.562475C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.465C>T	ENSP00000516315.1:p.Ala155=
ENST00000706272.1:c.548C>T
ENST00000304623.13:c.1476C>T MANE Select	ENSP00000307134.8:p.Ala492=
ENST00000304623.12:c.1476C>T	ENSP00000307134.8:p.Ala492=
ENST00000495388.6:n.561C>T
ENST00000503622.5:c.465C>T	ENSP00000426887.1:p.Ala155=
ENST00000504354.5:n.515C>T
ENST00000504499.5:c.*215C>T	ENSP00000421000.1:n.*215C>T
ENST00000511377.5:c.1203C>T	ENSP00000426510.1:p.Ala401=
ENST00000513588.5:c.738C>T	ENSP00000421093.1:p.Ala246=
NM_001288715.1:c.1203C>T	NP_001275644.1:p.Ala401=
NM_001288716.1:c.465C>T	NP_001275645.1:p.Ala155=
NM_001288717.1:c.177C>T	NP_001275646.1:p.Ala59=
NM_001332.3:c.1476C>T	NP_001323.1:p.Ala492=
NR_109988.1:n.928C>T
XM_005248251.2:c.1476C>T	XP_005248308.1:p.Ala492=
XM_005248252.1:c.1434C>T	XP_005248309.1:p.Ala478=
XM_005248253.1:c.1203C>T	XP_005248310.1:p.Ala401=
XM_011513967.1:c.1203C>T	XP_011512269.1:p.Ala401=
NM_001364128.1:c.465C>T	NP_001351057.1:p.Ala155=
XM_005248251.3:c.1476C>T	XP_005248308.1:p.Ala492=
XM_005248252.2:c.1434C>T	XP_005248309.1:p.Ala478=
XM_011513967.2:c.1203C>T	XP_011512269.1:p.Ala401=
XM_017009072.1:c.738C>T	XP_016864561.1:p.Ala246=
XM_017009073.1:c.696C>T	XP_016864562.1:p.Ala232=
XM_017009074.1:c.738C>T	XP_016864563.1:p.Ala246=
XM_017009075.2:c.465C>T	XP_016864564.1:p.Ala155=
XM_024454368.1:c.-44+18172C>T	XP_024310136.1:n.-44+18172C>T
NM_001332.4:c.1476C>T MANE Select	NP_001323.1:p.Ala492=
NM_001288717.2:c.177C>T	NP_001275646.1:p.Ala59=
NR_109988.2:n.1331C>T
NM_001364128.2:c.465C>T	NP_001351057.1:p.Ala155=