Canonical Allele Identifier: CA724956493

Gene: CDH13

Linked Data

• dbSNP Id: rs1268625659
• MyVariant Identifiers: chr16:g.83527689_83527690del (hg19) ; chr16:g.83494084_83494085del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83494084_83494085del , CM000678.2:g.83494084_83494085del	GRCh38
NC_000016.9:g.83527689_83527690del , CM000678.1:g.83527689_83527690del	GRCh37
NC_000016.8:g.82085190_82085191del	NCBI36
NG_052819.1:g.872291_872292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.960+7429_960+7430del MANE Select	ENSP00000479395.1:n.960+7429_960+7430del
ENST00000268613.14:c.1101+7429_1101+7430del	ENSP00000268613.10:n.1101+7429_1101+7430del
ENST00000428848.7:c.843+7429_843+7430del	ENSP00000394557.3:n.843+7429_843+7430del
ENST00000539548.6:c.*592+7429_*592+7430del	ENSP00000442225.2:n.*592+7429_*592+7430del
ENST00000566620.5:c.924+7429_924+7430del	ENSP00000454435.3:n.924+7429_924+7430del
ENST00000567109.5:c.960+7429_960+7430del	ENSP00000479395.1:n.960+7429_960+7430del
ENST00000622885.4:c.804+7429_804+7430del	ENSP00000483719.1:n.804+7429_804+7430del
NM_001220488.1:c.1101+7429_1101+7430del	NP_001207417.1:n.1101+7429_1101+7430del
NM_001220489.1:c.843+7429_843+7430del	NP_001207418.1:n.843+7429_843+7430del
NM_001220490.1:c.198+7429_198+7430del	NP_001207419.1:n.198+7429_198+7430del
NM_001257.4:c.960+7429_960+7430del	NP_001248.1:n.960+7429_960+7430del
XM_011522804.1:c.657+7429_657+7430del	XP_011521106.1:n.657+7429_657+7430del
XM_011522805.1:c.1101+7429_1101+7430del	XP_011521107.1:n.1101+7429_1101+7430del
XM_011522804.3:c.657+7429_657+7430del	XP_011521106.1:n.657+7429_657+7430del
XM_017022848.2:c.1101+7429_1101+7430del	XP_016878337.1:n.1101+7429_1101+7430del
NM_001257.5:c.960+7429_960+7430del MANE Select	NP_001248.1:n.960+7429_960+7430del
NM_001220488.2:c.1101+7429_1101+7430del	NP_001207417.1:n.1101+7429_1101+7430del
NM_001220489.2:c.843+7429_843+7430del	NP_001207418.1:n.843+7429_843+7430del
NM_001220490.2:c.198+7429_198+7430del	NP_001207419.1:n.198+7429_198+7430del