Canonical Allele Identifier: CA396195933

Gene: CDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66402687C>T , CM000678.2:g.66402687C>T	GRCh38
NC_000016.9:g.66436590C>T , CM000678.1:g.66436590C>T	GRCh37
NC_000016.8:g.64994091C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341529.8:c.1873C>T MANE Select	ENSP00000344115.3:p.Arg625Trp
ENST00000649567.1:c.1873C>T	ENSP00000497290.1:p.Arg625Trp
ENST00000341529.7:c.1873C>T	ENSP00000344115.3:p.Arg625Trp
ENST00000539168.1:c.190C>T	ENSP00000461880.1:p.Arg64Trp
ENST00000565334.5:c.*996C>T	ENSP00000456028.1:n.*996C>T
ENST00000614547.4:c.1528C>T	ENSP00000479381.1:p.Arg510Trp
NM_001795.3:c.1873C>T	NP_001786.2:p.Arg625Trp
XM_011522801.1:c.1900C>T	XP_011521103.1:p.Arg634Trp
NM_001795.4:c.1873C>T	NP_001786.2:p.Arg625Trp
XM_011522801.2:c.1900C>T	XP_011521103.1:p.Arg634Trp
XM_024450133.1:c.1900C>T	XP_024305901.1:p.Arg634Trp
NM_001795.5:c.1873C>T MANE Select	NP_001786.2:p.Arg625Trp