Canonical Allele Identifier: CA2292176491

Gene: CDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.28037661A= , CM000680.2:g.28037661A=	GRCh38
NC_000018.9:g.25617625A= , CM000680.1:g.25617625A=	GRCh37
NC_000018.8:g.23871623A=	NCBI36
NG_011959.1:g.144821T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001792.5:c.173-23752T= MANE Select	NP_001783.2:n.173-23752T=
ENST00000269141.8:c.173-23752T= MANE Select	ENSP00000269141.3:n.173-23752T=
NM_001792.3:c.173-23752T=	NP_001783.2:n.173-23752T=
NM_001792.4:c.173-23752T=	NP_001783.2:n.173-23752T=
ENST00000269141.7:c.173-23752T=	ENSP00000269141.3:n.173-23752T=
ENST00000413878.1:c.-83-23752T=	ENSP00000414269.1:n.-83-23752T=
ENST00000413878.2:c.-83-23752T=	ENSP00000414269.2:n.-83-23752T=
ENST00000418492.5:c.19+7750T=	ENSP00000411360.1:n.19+7750T=
ENST00000430882.5:c.-83-23752T=	ENSP00000412120.1:n.-83-23752T=
ENST00000430882.6:c.-83-23752T=	ENSP00000412120.2:n.-83-23752T=
ENST00000675708.1:c.-83-23752T=	ENSP00000501654.1:n.-83-23752T=
ENST00000676445.1:c.-83-23752T=	ENSP00000502206.1:n.-83-23752T=
XM_005258181.2:c.119-23752T=	XP_005258238.1:n.119-23752T=
XM_011525787.1:c.119-23752T=	XP_011524089.1:n.119-23752T=
XM_011525788.1:c.-83-23752T=	XP_011524090.1:n.-83-23752T=
XM_017025514.2:c.173-23752T=	XP_016881003.1:n.173-23752T=