Canonical Allele Identifier: CA3200984

Gene: CTNND2

Linked Data

• dbSNP Id: rs763852209
• ExAC: 5:11384922 CGAG / C
• gnomAD v2: 5-11384922-CGAG-C
• gnomAD v4: 5-11384810-CGAG-C
• MyVariant Identifiers: chr5:g.11384923_11384925del (hg19) ; chr5:g.11384811_11384813del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11384817_11384819del , CM000667.2:g.11384817_11384819del	GRCh38
NC_000005.9:g.11384929_11384931del , CM000667.1:g.11384929_11384931del	GRCh37
NC_000005.8:g.11437929_11437931del	NCBI36
NG_023544.1:g.524186_524188del
NG_023544.2:g.524186_524188del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.167-19923_167-19921del	ENSP00000516315.1:n.167-19923_167-19921del
ENST00000706272.1:c.101_103del
ENST00000304623.13:c.1029_1031del MANE Select	ENSP00000307134.8:p.Ser344del
ENST00000304623.12:c.1029_1031del	ENSP00000307134.8:p.Ser344del
ENST00000502551.5:c.398-19923_398-19921del	ENSP00000422389.1:n.398-19923_398-19921del
ENST00000503622.5:c.167-19923_167-19921del	ENSP00000426887.1:n.167-19923_167-19921del
ENST00000504354.5:n.217-19923_217-19921del
ENST00000504499.5:c.612+12218_612+12220del	ENSP00000421000.1:n.612+12218_612+12220del
ENST00000506735.1:n.100_102del
ENST00000507430.1:n.125_127del
ENST00000511278.5:n.542-19923_542-19921del
ENST00000511377.5:c.756_758del	ENSP00000426510.1:p.Ser253del
ENST00000513588.5:c.440-19923_440-19921del	ENSP00000421093.1:n.440-19923_440-19921del
NM_001288715.1:c.756_758del	NP_001275644.1:p.Ser253del
NM_001288716.1:c.167-19923_167-19921del	NP_001275645.1:n.167-19923_167-19921del
NM_001288717.1:c.-123+12218_-123+12220del	NP_001275646.1:n.-123+12218_-123+12220del
NM_001332.3:c.1029_1031del	NP_001323.1:p.Ser344del
NR_109988.1:n.630-19923_630-19921del
XM_005248251.2:c.1029_1031del	XP_005248308.1:p.Ser344del
XM_005248252.1:c.987_989del	XP_005248309.1:p.Ser330del
XM_005248253.1:c.756_758del	XP_005248310.1:p.Ser253del
XM_011513967.1:c.756_758del	XP_011512269.1:p.Ser253del
NM_001364128.1:c.167-19923_167-19921del	NP_001351057.1:n.167-19923_167-19921del
XM_005248251.3:c.1029_1031del	XP_005248308.1:p.Ser344del
XM_005248252.2:c.987_989del	XP_005248309.1:p.Ser330del
XM_011513967.2:c.756_758del	XP_011512269.1:p.Ser253del
XM_017009072.1:c.440-19923_440-19921del	XP_016864561.1:n.440-19923_440-19921del
XM_017009073.1:c.398-19923_398-19921del	XP_016864562.1:n.398-19923_398-19921del
XM_017009074.1:c.440-19923_440-19921del	XP_016864563.1:n.440-19923_440-19921del
XM_017009075.2:c.167-19923_167-19921del	XP_016864564.1:n.167-19923_167-19921del
XM_024454368.1:c.-387_-385del	XP_024310136.1:n.-387_-385del
NM_001332.4:c.1029_1031del MANE Select	NP_001323.1:p.Ser344del
NM_001288717.2:c.-123+12218_-123+12220del	NP_001275646.1:n.-123+12218_-123+12220del
NR_109988.2:n.1033-19923_1033-19921del
NM_001364128.2:c.167-19923_167-19921del	NP_001351057.1:n.167-19923_167-19921del