Canonical Allele Identifier: CA443541160

Gene: CTNND2

Linked Data

• gnomAD v4: 5-11346500-C-G
• MyVariant Identifiers: chr5:g.11346612C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.11346500C>G , CM000667.2:g.11346500C>G	GRCh38
NC_000005.9:g.11346612C>G , CM000667.1:g.11346612C>G	GRCh37
NC_000005.8:g.11399612C>G	NCBI36
NG_023544.1:g.562499G>C
NG_023544.2:g.562499G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706271.1:c.489G>C	ENSP00000516315.1:p.Ala163=
ENST00000706272.1:c.572G>C
ENST00000304623.13:c.1500G>C MANE Select	ENSP00000307134.8:p.Ala500=
ENST00000304623.12:c.1500G>C	ENSP00000307134.8:p.Ala500=
ENST00000495388.6:n.585G>C
ENST00000503622.5:c.489G>C	ENSP00000426887.1:p.Ala163=
ENST00000504354.5:n.539G>C
ENST00000504499.5:c.*239G>C	ENSP00000421000.1:n.*239G>C
ENST00000511377.5:c.1227G>C	ENSP00000426510.1:p.Ala409=
ENST00000513588.5:c.762G>C	ENSP00000421093.1:p.Ala254=
NM_001288715.1:c.1227G>C	NP_001275644.1:p.Ala409=
NM_001288716.1:c.489G>C	NP_001275645.1:p.Ala163=
NM_001288717.1:c.201G>C	NP_001275646.1:p.Ala67=
NM_001332.3:c.1500G>C	NP_001323.1:p.Ala500=
NR_109988.1:n.952G>C
XM_005248251.2:c.1500G>C	XP_005248308.1:p.Ala500=
XM_005248252.1:c.1458G>C	XP_005248309.1:p.Ala486=
XM_005248253.1:c.1227G>C	XP_005248310.1:p.Ala409=
XM_011513967.1:c.1227G>C	XP_011512269.1:p.Ala409=
NM_001364128.1:c.489G>C	NP_001351057.1:p.Ala163=
XM_005248251.3:c.1500G>C	XP_005248308.1:p.Ala500=
XM_005248252.2:c.1458G>C	XP_005248309.1:p.Ala486=
XM_011513967.2:c.1227G>C	XP_011512269.1:p.Ala409=
XM_017009072.1:c.762G>C	XP_016864561.1:p.Ala254=
XM_017009073.1:c.720G>C	XP_016864562.1:p.Ala240=
XM_017009074.1:c.762G>C	XP_016864563.1:p.Ala254=
XM_017009075.2:c.489G>C	XP_016864564.1:p.Ala163=
XM_024454368.1:c.-44+18196G>C	XP_024310136.1:n.-44+18196G>C
NM_001332.4:c.1500G>C MANE Select	NP_001323.1:p.Ala500=
NM_001288717.2:c.201G>C	NP_001275646.1:p.Ala67=
NR_109988.2:n.1355G>C
NM_001364128.2:c.489G>C	NP_001351057.1:p.Ala163=