Canonical Allele Identifier: CA623995702
Gene: CDH13 HGNC NCBI

Linked Data

dbSNP Id: rs1391095967

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.83237194_83237196del , CM000678.2:g.83237194_83237196del GRCh38
NC_000016.9:g.83270799_83270801del , CM000678.1:g.83270799_83270801del GRCh37
NC_000016.8:g.81828300_81828302del NCBI36
NG_052819.1:g.615401_615403del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567109.6:c.636+19697_636+19699del MANE Select ENSP00000479395.1:n.636+19697_636+19699del
ENST00000268613.14:c.777+19697_777+19699del ENSP00000268613.10:n.777+19697_777+19699del
ENST00000428848.7:c.519+19697_519+19699del ENSP00000394557.3:n.519+19697_519+19699del
ENST00000539548.6:c.*268+19697_*268+19699del ENSP00000442225.2:n.*268+19697_*268+19699del
ENST00000566620.5:c.600+19697_600+19699del ENSP00000454435.3:n.600+19697_600+19699del
ENST00000567109.5:c.636+19697_636+19699del ENSP00000479395.1:n.636+19697_636+19699del
ENST00000569454.1:n.553+19697_553+19699del
ENST00000622885.4:c.480+19697_480+19699del ENSP00000483719.1:n.480+19697_480+19699del
NM_001220488.1:c.777+19697_777+19699del NP_001207417.1:n.777+19697_777+19699del
NM_001220489.1:c.519+19697_519+19699del NP_001207418.1:n.519+19697_519+19699del
NM_001220490.1:c.-127+19697_-127+19699del NP_001207419.1:n.-127+19697_-127+19699del
NM_001257.4:c.636+19697_636+19699del NP_001248.1:n.636+19697_636+19699del
XM_011522804.1:c.333+19697_333+19699del XP_011521106.1:n.333+19697_333+19699del
XM_011522805.1:c.777+19697_777+19699del XP_011521107.1:n.777+19697_777+19699del
XM_011522804.3:c.333+19697_333+19699del XP_011521106.1:n.333+19697_333+19699del
XM_017022848.2:c.777+19697_777+19699del XP_016878337.1:n.777+19697_777+19699del
NM_001257.5:c.636+19697_636+19699del MANE Select NP_001248.1:n.636+19697_636+19699del
NM_001220488.2:c.777+19697_777+19699del NP_001207417.1:n.777+19697_777+19699del
NM_001220489.2:c.519+19697_519+19699del NP_001207418.1:n.519+19697_519+19699del
NM_001220490.2:c.-127+19697_-127+19699del NP_001207419.1:n.-127+19697_-127+19699del