Canonical Allele Identifier: CA2549153959

Gene: CDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66398434_66398435insGG , CM000678.2:g.66398434_66398435insGG	GRCh38
NC_000016.9:g.66432337_66432338insGG , CM000678.1:g.66432337_66432338insGG	GRCh37
NC_000016.8:g.64989838_64989839insGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341529.8:c.1486-22_1486-21insGG MANE Select	ENSP00000344115.3:n.1486-22_1486-21insGG
ENST00000649567.1:c.1486-22_1486-21insGG	ENSP00000497290.1:n.1486-22_1486-21insGG
ENST00000341529.7:c.1486-22_1486-21insGG	ENSP00000344115.3:n.1486-22_1486-21insGG
ENST00000539168.1:c.-198-22_-198-21insGG	ENSP00000461880.1:n.-198-22_-198-21insGG
ENST00000565334.5:c.*609-22_*609-21insGG	ENSP00000456028.1:n.*609-22_*609-21insGG
ENST00000614547.4:c.1141-22_1141-21insGG	ENSP00000479381.1:n.1141-22_1141-21insGG
NM_001795.3:c.1486-22_1486-21insGG	NP_001786.2:n.1486-22_1486-21insGG
XM_011522801.1:c.1513-22_1513-21insGG	XP_011521103.1:n.1513-22_1513-21insGG
NM_001795.4:c.1486-22_1486-21insGG	NP_001786.2:n.1486-22_1486-21insGG
XM_011522801.2:c.1513-22_1513-21insGG	XP_011521103.1:n.1513-22_1513-21insGG
XM_024450133.1:c.1513-22_1513-21insGG	XP_024305901.1:n.1513-22_1513-21insGG
NM_001795.5:c.1486-22_1486-21insGG MANE Select	NP_001786.2:n.1486-22_1486-21insGG