Canonical Allele Identifier: CA396194490

Gene: CDH5

Linked Data

• MyVariant Identifiers: chr16:g.66432461C>G (hg19) ; chr16:g.66398558C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66398558C>G , CM000678.2:g.66398558C>G	GRCh38
NC_000016.9:g.66432461C>G , CM000678.1:g.66432461C>G	GRCh37
NC_000016.8:g.64989962C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341529.8:c.1588C>G MANE Select	ENSP00000344115.3:p.His530Asp
ENST00000649567.1:c.1588C>G	ENSP00000497290.1:p.His530Asp
ENST00000341529.7:c.1588C>G	ENSP00000344115.3:p.His530Asp
ENST00000539168.1:c.-96C>G	ENSP00000461880.1:n.-96C>G
ENST00000565334.5:c.*711C>G	ENSP00000456028.1:n.*711C>G
ENST00000614547.4:c.1243C>G	ENSP00000479381.1:p.His415Asp
NM_001795.3:c.1588C>G	NP_001786.2:p.His530Asp
XM_011522801.1:c.1615C>G	XP_011521103.1:p.His539Asp
NM_001795.4:c.1588C>G	NP_001786.2:p.His530Asp
XM_011522801.2:c.1615C>G	XP_011521103.1:p.His539Asp
XM_024450133.1:c.1615C>G	XP_024305901.1:p.His539Asp
NM_001795.5:c.1588C>G MANE Select	NP_001786.2:p.His530Asp