Canonical Allele Identifier: CA2228852466

Gene: CDH5

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.66398543A= , CM000678.2:g.66398543A=	GRCh38
NC_000016.9:g.66432446A= , CM000678.1:g.66432446A=	GRCh37
NC_000016.8:g.64989947A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341529.8:c.1573A= MANE Select	ENSP00000344115.3:p.Thr525=
ENST00000649567.1:c.1573A=	ENSP00000497290.1:p.Thr525=
ENST00000341529.7:c.1573A=	ENSP00000344115.3:p.Thr525=
ENST00000539168.1:c.-111A=	ENSP00000461880.1:n.-111A=
ENST00000565334.5:c.*696A=	ENSP00000456028.1:n.*696A=
ENST00000614547.4:c.1228A=	ENSP00000479381.1:p.Thr410=
NM_001795.3:c.1573A=	NP_001786.2:p.Thr525=
XM_011522801.1:c.1600A=	XP_011521103.1:p.Thr534=
NM_001795.4:c.1573A=	NP_001786.2:p.Thr525=
XM_011522801.2:c.1600A=	XP_011521103.1:p.Thr534=
XM_024450133.1:c.1600A=	XP_024305901.1:p.Thr534=
NM_001795.5:c.1573A= MANE Select	NP_001786.2:p.Thr525=