Canonical Allele Identifier: CA2292154495

Gene: CDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.27989094A= , CM000680.2:g.27989094A=	GRCh38
NC_000018.9:g.25569058A= , CM000680.1:g.25569058A=	GRCh37
NC_000018.8:g.23823056A=	NCBI36
NG_011959.1:g.193388T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001792.5:c.1599-428T= MANE Select	NP_001783.2:n.1599-428T=
ENST00000269141.8:c.1599-428T= MANE Select	ENSP00000269141.3:n.1599-428T=
NM_001308176.1:c.1506-428T=	NP_001295105.1:n.1506-428T=
NM_001308176.2:c.1506-428T=	NP_001295105.1:n.1506-428T=
NM_001792.3:c.1599-428T=	NP_001783.2:n.1599-428T=
NM_001792.4:c.1599-428T=	NP_001783.2:n.1599-428T=
ENST00000269141.7:c.1599-428T=	ENSP00000269141.3:n.1599-428T=
ENST00000399380.7:c.1506-428T=	ENSP00000382312.3:n.1506-428T=
ENST00000413878.2:c.1344-428T=	ENSP00000414269.2:n.1344-428T=
ENST00000430882.6:c.1344-428T=	ENSP00000412120.2:n.1344-428T=
ENST00000675173.1:c.236-428T=
ENST00000675708.1:c.1344-428T=	ENSP00000501654.1:n.1344-428T=
ENST00000676041.1:n.1330-428T=
ENST00000676445.1:c.1344-428T=	ENSP00000502206.1:n.1344-428T=
XM_005258181.2:c.1545-428T=	XP_005258238.1:n.1545-428T=
XM_011525787.1:c.1545-428T=	XP_011524089.1:n.1545-428T=
XM_011525788.1:c.1344-428T=	XP_011524090.1:n.1344-428T=
XM_017025514.2:c.1599-428T=	XP_016881003.1:n.1599-428T=