Canonical Allele Identifier: CA2292147023

Gene: CDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.27971997G= , CM000680.2:g.27971997G=	GRCh38
NC_000018.9:g.25551961G= , CM000680.1:g.25551961G=	GRCh37
NC_000018.8:g.23805959G=	NCBI36
NG_011959.1:g.210485C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001792.5:c.2350-8476C= MANE Select	NP_001783.2:n.2350-8476C=
ENST00000269141.8:c.2350-8476C= MANE Select	ENSP00000269141.3:n.2350-8476C=
NM_001308176.1:c.2257-8476C=	NP_001295105.1:n.2257-8476C=
NM_001308176.2:c.2257-8476C=	NP_001295105.1:n.2257-8476C=
NM_001792.3:c.2350-8476C=	NP_001783.2:n.2350-8476C=
NM_001792.4:c.2350-8476C=	NP_001783.2:n.2350-8476C=
ENST00000269141.7:c.2350-8476C=	ENSP00000269141.3:n.2350-8476C=
ENST00000399380.7:c.2257-8476C=	ENSP00000382312.3:n.2257-8476C=
ENST00000430882.6:c.2095-8476C=	ENSP00000412120.2:n.2095-8476C=
ENST00000675173.1:c.987-8476C=
ENST00000675688.1:c.302-8476C=
ENST00000675708.1:c.2095-6015C=	ENSP00000501654.1:n.2095-6015C=
ENST00000676041.1:n.2081-8476C=
ENST00000676445.1:c.2095-8476C=	ENSP00000502206.1:n.2095-8476C=
XM_005258181.2:c.2296-8476C=	XP_005258238.1:n.2296-8476C=
XM_011525787.1:c.2296-8476C=	XP_011524089.1:n.2296-8476C=
XM_011525788.1:c.2095-8476C=	XP_011524090.1:n.2095-8476C=
XM_017025514.2:c.2350-8476C=	XP_016881003.1:n.2350-8476C=