Canonical Allele Identifier: CA919728744

Gene: CDH5

Linked Data

• dbSNP Id: rs1555513649

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66398416_66398422dup , CM000678.2:g.66398416_66398422dup	GRCh38
NC_000016.9:g.66432319_66432325dup , CM000678.1:g.66432319_66432325dup	GRCh37
NC_000016.8:g.64989820_64989826dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341529.8:c.1486-40_1486-34dup MANE Select	ENSP00000344115.3:n.1486-40_1486-34dup
ENST00000649567.1:c.1486-40_1486-34dup	ENSP00000497290.1:n.1486-40_1486-34dup
ENST00000341529.7:c.1486-40_1486-34dup	ENSP00000344115.3:n.1486-40_1486-34dup
ENST00000539168.1:c.-198-40_-198-34dup	ENSP00000461880.1:n.-198-40_-198-34dup
ENST00000565334.5:c.*609-40_*609-34dup	ENSP00000456028.1:n.*609-40_*609-34dup
ENST00000614547.4:c.1141-40_1141-34dup	ENSP00000479381.1:n.1141-40_1141-34dup
NM_001795.3:c.1486-40_1486-34dup	NP_001786.2:n.1486-40_1486-34dup
XM_011522801.1:c.1513-40_1513-34dup	XP_011521103.1:n.1513-40_1513-34dup
NM_001795.4:c.1486-40_1486-34dup	NP_001786.2:n.1486-40_1486-34dup
XM_011522801.2:c.1513-40_1513-34dup	XP_011521103.1:n.1513-40_1513-34dup
XM_024450133.1:c.1513-40_1513-34dup	XP_024305901.1:n.1513-40_1513-34dup
NM_001795.5:c.1486-40_1486-34dup MANE Select	NP_001786.2:n.1486-40_1486-34dup