Canonical Allele Identifier: CA2739275545

Gene: CNTN2

Linked Data

• ClinVar Variation Id: 2888349
• ClinVar RCV Id: RCV003742581

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.205058009_205058010delinsTT , CM000663.2:g.205058009_205058010delinsTT	GRCh38
NC_000001.10:g.205027137_205027138delinsTT , CM000663.1:g.205027137_205027138delinsTT	GRCh37
NC_000001.9:g.203293760_203293761delinsTT	NCBI36
NG_033845.1:g.19798_19799delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331830.7:c.159_160delinsTT MANE Select	ENSP00000330633.4:p.Thr54Ter
ENST00000532366.2:c.*746_*747delinsTT	ENSP00000491665.1:n.*746_*747delinsTT
ENST00000636809.2:n.447_448delinsTT
ENST00000638378.1:c.159_160delinsTT	ENSP00000492617.1:p.Thr54Ter
ENST00000639302.1:c.159_160delinsTT	ENSP00000491671.1:p.Thr54Ter
ENST00000639971.1:c.159_160delinsTT	ENSP00000491959.1:p.Thr54Ter
ENST00000640326.1:c.159_160delinsTT	ENSP00000492495.1:p.Thr54Ter
ENST00000640352.1:c.*746_*747delinsTT	ENSP00000491080.1:n.*746_*747delinsTT
ENST00000640428.1:c.159_160delinsTT	ENSP00000491474.1:p.Thr54Ter
ENST00000331830.4:c.159_160delinsTT	ENSP00000330633.4:p.Thr54Ter
ENST00000532366.1:n.272_273delinsTT
NM_005076.3:c.159_160delinsTT	NP_005067.1:p.Thr54Ter
XM_011509925.1:c.144_145delinsTT	XP_011508227.1:p.Thr49Ter
NM_001346083.1:c.159_160delinsTT	NP_001333012.1:p.Thr54Ter
NM_005076.4:c.159_160delinsTT	NP_005067.1:p.Thr54Ter
NR_144350.1:n.516_517delinsTT
XM_017002198.1:c.159_160delinsTT	XP_016857687.1:p.Thr54Ter
XM_017002199.2:c.144_145delinsTT	XP_016857688.1:p.Thr49Ter
XM_024449386.1:c.198_199delinsTT	XP_024305154.1:p.Thr67Ter
XM_024449387.1:c.-380_-379delinsTT	XP_024305155.1:n.-380_-379delinsTT
XM_024449388.1:c.-380_-379delinsTT	XP_024305156.1:n.-380_-379delinsTT
XM_024449389.1:c.198_199delinsTT	XP_024305157.1:p.Thr67Ter
NM_005076.5:c.159_160delinsTT MANE Select	NP_005067.1:p.Thr54Ter
NM_001346083.2:c.159_160delinsTT	NP_001333012.1:p.Thr54Ter
NR_144350.2:n.428_429delinsTT