Canonical Allele Identifier: CA645592444

Gene: CDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66402686_66402687delinsTT , CM000678.2:g.66402686_66402687delinsTT	GRCh38
NC_000016.9:g.66436589_66436590delinsTT , CM000678.1:g.66436589_66436590delinsTT	GRCh37
NC_000016.8:g.64994090_64994091delinsTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341529.8:c.1872_1873delinsTT MANE Select	ENSP00000344115.3:p.Arg625Trp
ENST00000649567.1:c.1872_1873delinsTT	ENSP00000497290.1:p.Arg625Trp
ENST00000341529.7:c.1872_1873delinsTT	ENSP00000344115.3:p.Arg625Trp
ENST00000539168.1:c.189_190delinsTT	ENSP00000461880.1:p.Arg64Trp
ENST00000565334.5:c.*995_*996delinsTT	ENSP00000456028.1:n.*995_*996delinsTT
ENST00000614547.4:c.1527_1528delinsTT	ENSP00000479381.1:p.Arg510Trp
NM_001795.3:c.1872_1873delinsTT	NP_001786.2:p.Arg625Trp
XM_011522801.1:c.1899_1900delinsTT	XP_011521103.1:p.Arg634Trp
NM_001795.4:c.1872_1873delinsTT	NP_001786.2:p.Arg625Trp
XM_011522801.2:c.1899_1900delinsTT	XP_011521103.1:p.Arg634Trp
XM_024450133.1:c.1899_1900delinsTT	XP_024305901.1:p.Arg634Trp
NM_001795.5:c.1872_1873delinsTT MANE Select	NP_001786.2:p.Arg625Trp