Canonical Allele Identifier: CA208996842

Gene: CTNNA3

Linked Data

• dbSNP Id: rs924094793
• gnomAD v2: 10-68085311-GCTT-G
• gnomAD v3: 10-66325553-GCTT-G
• gnomAD v4: 10-66325553-GCTT-G
• MyVariant Identifiers: chr10:g.68085312_68085314del (hg19) ; chr10:g.66325554_66325556del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.66325557_66325559del , CM000672.2:g.66325557_66325559del	GRCh38
NC_000010.10:g.68085315_68085317del , CM000672.1:g.68085315_68085317del	GRCh37
NC_000010.9:g.67755321_67755323del	NCBI36
NG_034072.1:g.1375636_1375638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682758.1:c.1733-44935_1733-44933del	ENSP00000508047.1:n.1733-44935_1733-44933del
ENST00000682945.1:c.1532-44935_1532-44933del	ENSP00000506843.1:n.1532-44935_1532-44933del
ENST00000683624.1:c.*1272-44935_*1272-44933del	ENSP00000507406.1:n.*1272-44935_*1272-44933del
ENST00000683963.1:c.*1257-44935_*1257-44933del	ENSP00000507029.1:n.*1257-44935_*1257-44933del
ENST00000684154.1:c.1733-44935_1733-44933del	ENSP00000508371.1:n.1733-44935_1733-44933del
ENST00000433211.7:c.1733-44935_1733-44933del MANE Select	ENSP00000389714.1:n.1733-44935_1733-44933del
ENST00000433211.6:c.1733-44935_1733-44933del	ENSP00000389714.1:n.1733-44935_1733-44933del
NM_001127384.2:c.1733-44935_1733-44933del	NP_001120856.1:n.1733-44935_1733-44933del
NM_013266.3:c.1733-44935_1733-44933del	NP_037398.2:n.1733-44935_1733-44933del
XM_005269717.2:c.1769-44935_1769-44933del	XP_005269774.1:n.1769-44935_1769-44933del
XM_011539721.1:c.1838-44935_1838-44933del	XP_011538023.1:n.1838-44935_1838-44933del
XM_011539722.1:c.1838-44935_1838-44933del	XP_011538024.1:n.1838-44935_1838-44933del
XM_011539723.1:c.1802-44935_1802-44933del	XP_011538025.1:n.1802-44935_1802-44933del
XM_011539724.1:c.1802-44935_1802-44933del	XP_011538026.1:n.1802-44935_1802-44933del
XM_011539725.1:c.1802-44935_1802-44933del	XP_011538027.1:n.1802-44935_1802-44933del
XM_011539726.1:c.1769-44935_1769-44933del	XP_011538028.1:n.1769-44935_1769-44933del
XM_011539727.1:c.1733-44935_1733-44933del	XP_011538029.1:n.1733-44935_1733-44933del
XM_017016151.1:c.1802-44935_1802-44933del	XP_016871640.1:n.1802-44935_1802-44933del
XM_017016152.1:c.1958-44935_1958-44933del	XP_016871641.1:n.1958-44935_1958-44933del
XM_017016153.1:c.1769-44935_1769-44933del	XP_016871642.1:n.1769-44935_1769-44933del
XM_017016154.1:c.950-44935_950-44933del	XP_016871643.1:n.950-44935_950-44933del
XM_017016155.2:c.950-44935_950-44933del	XP_016871644.1:n.950-44935_950-44933del
XM_017016156.1:c.950-44935_950-44933del	XP_016871645.1:n.950-44935_950-44933del
XM_017016157.2:c.638-44935_638-44933del	XP_016871646.1:n.638-44935_638-44933del
NM_013266.4:c.1733-44935_1733-44933del MANE Select	NP_037398.2:n.1733-44935_1733-44933del
NM_001127384.3:c.1733-44935_1733-44933del	NP_001120856.1:n.1733-44935_1733-44933del