Canonical Allele Identifier: CA801830397

Gene: CTNND2

Linked Data

• dbSNP Id: rs1439322442
• gnomAD v3: 5-11084509-T-G
• gnomAD v4: 5-11084509-T-G
• MyVariant Identifiers: chr5:g.11084621T>G (hg19) ; chr5:g.11084509T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11084509T>G , CM000667.2:g.11084509T>G	GRCh38
NC_000005.9:g.11084621T>G , CM000667.1:g.11084621T>G	GRCh37
NC_000005.8:g.11137621T>G	NCBI36
NG_023544.1:g.824490A>C
NG_023544.2:g.824490A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706271.1:c.1627-554A>C	ENSP00000516315.1:n.1627-554A>C
ENST00000706272.1:c.1710-554A>C
ENST00000304623.13:c.2638-1663A>C MANE Select	ENSP00000307134.8:n.2638-1663A>C
ENST00000304623.12:c.2638-1663A>C	ENSP00000307134.8:n.2638-1663A>C
ENST00000458100.6:c.-76-1663A>C	ENSP00000391155.3:n.-76-1663A>C
ENST00000495388.6:n.1723-1663A>C
ENST00000503622.5:c.1627-1663A>C	ENSP00000426887.1:n.1627-1663A>C
ENST00000504499.5:c.*1377-1663A>C	ENSP00000421000.1:n.*1377-1663A>C
ENST00000511377.5:c.2365-1663A>C	ENSP00000426510.1:n.2365-1663A>C
ENST00000513588.5:c.1900-554A>C	ENSP00000421093.1:n.1900-554A>C
NM_001288715.1:c.2365-1663A>C	NP_001275644.1:n.2365-1663A>C
NM_001288716.1:c.1627-1663A>C	NP_001275645.1:n.1627-1663A>C
NM_001288717.1:c.1339-1663A>C	NP_001275646.1:n.1339-1663A>C
NM_001332.3:c.2638-1663A>C	NP_001323.1:n.2638-1663A>C
NR_109988.1:n.2090-554A>C
XM_005248251.2:c.2638-554A>C	XP_005248308.1:n.2638-554A>C
XM_005248252.1:c.2596-554A>C	XP_005248309.1:n.2596-554A>C
XM_005248253.1:c.2365-554A>C	XP_005248310.1:n.2365-554A>C
XM_011513967.1:c.2365-554A>C	XP_011512269.1:n.2365-554A>C
NM_001364128.1:c.1627-554A>C	NP_001351057.1:n.1627-554A>C
XM_005248251.3:c.2638-554A>C	XP_005248308.1:n.2638-554A>C
XM_005248252.2:c.2596-554A>C	XP_005248309.1:n.2596-554A>C
XM_011513967.2:c.2365-554A>C	XP_011512269.1:n.2365-554A>C
XM_017009072.1:c.1900-554A>C	XP_016864561.1:n.1900-554A>C
XM_017009073.1:c.1858-554A>C	XP_016864562.1:n.1858-554A>C
XM_017009074.1:c.1900-1663A>C	XP_016864563.1:n.1900-1663A>C
XM_017009075.2:c.1627-554A>C	XP_016864564.1:n.1627-554A>C
XM_024454368.1:c.967-1663A>C	XP_024310136.1:n.967-1663A>C
NM_001332.4:c.2638-1663A>C MANE Select	NP_001323.1:n.2638-1663A>C
NM_001288717.2:c.1339-1663A>C	NP_001275646.1:n.1339-1663A>C
NR_109988.2:n.2493-554A>C
NM_001364128.2:c.1627-554A>C	NP_001351057.1:n.1627-554A>C