Canonical Allele Identifier: CA725021547

Gene: CDH13

Linked Data

• dbSNP Id: rs1375644973
• MyVariant Identifiers: chr16:g.83709725_83709728del (hg19) ; chr16:g.83676120_83676123del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.83676122_83676125del , CM000678.2:g.83676122_83676125del	GRCh38
NC_000016.9:g.83709727_83709730del , CM000678.1:g.83709727_83709730del	GRCh37
NC_000016.8:g.82267228_82267231del	NCBI36
NG_052819.1:g.1054329_1054332del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567109.6:c.1285-2086_1285-2083del MANE Select	ENSP00000479395.1:n.1285-2086_1285-2083del
ENST00000268613.14:c.1426-2086_1426-2083del	ENSP00000268613.10:n.1426-2086_1426-2083del
ENST00000428848.7:c.1168-2086_1168-2083del	ENSP00000394557.3:n.1168-2086_1168-2083del
ENST00000539548.6:c.*917-2086_*917-2083del	ENSP00000442225.2:n.*917-2086_*917-2083del
ENST00000566620.5:c.1249-2086_1249-2083del	ENSP00000454435.3:n.1249-2086_1249-2083del
ENST00000567109.5:c.1285-2086_1285-2083del	ENSP00000479395.1:n.1285-2086_1285-2083del
ENST00000615627.1:c.205-2086_205-2083del	ENSP00000482651.1:n.205-2086_205-2083del
ENST00000622885.4:c.1129-2086_1129-2083del	ENSP00000483719.1:n.1129-2086_1129-2083del
NM_001220488.1:c.1426-2086_1426-2083del	NP_001207417.1:n.1426-2086_1426-2083del
NM_001220489.1:c.1168-2086_1168-2083del	NP_001207418.1:n.1168-2086_1168-2083del
NM_001220490.1:c.523-2086_523-2083del	NP_001207419.1:n.523-2086_523-2083del
NM_001257.4:c.1285-2086_1285-2083del	NP_001248.1:n.1285-2086_1285-2083del
XM_011522804.1:c.982-2086_982-2083del	XP_011521106.1:n.982-2086_982-2083del
XM_011522804.3:c.982-2086_982-2083del	XP_011521106.1:n.982-2086_982-2083del
XR_001752385.2:n.6466-8532_6466-8529del
NM_001257.5:c.1285-2086_1285-2083del MANE Select	NP_001248.1:n.1285-2086_1285-2083del
NM_001220488.2:c.1426-2086_1426-2083del	NP_001207417.1:n.1426-2086_1426-2083del
NM_001220489.2:c.1168-2086_1168-2083del	NP_001207418.1:n.1168-2086_1168-2083del
NM_001220490.2:c.523-2086_523-2083del	NP_001207419.1:n.523-2086_523-2083del