Canonical Allele Identifier: CA2292238095

Gene: CDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.28171702G= , CM000680.2:g.28171702G=	GRCh38
NC_000018.9:g.25751666G= , CM000680.1:g.25751666G=	GRCh37
NC_000018.8:g.24005664G=	NCBI36
NG_011959.1:g.10780C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001792.5:c.60+5261C= MANE Select	NP_001783.2:n.60+5261C=
ENST00000269141.8:c.60+5261C= MANE Select	ENSP00000269141.3:n.60+5261C=
NM_001792.3:c.60+5261C=	NP_001783.2:n.60+5261C=
NM_001792.4:c.60+5261C=	NP_001783.2:n.60+5261C=
ENST00000269141.7:c.60+5261C=	ENSP00000269141.3:n.60+5261C=
ENST00000413878.2:c.-343+5261C=	ENSP00000414269.2:n.-343+5261C=
ENST00000430882.6:c.-388+5261C=	ENSP00000412120.2:n.-388+5261C=
ENST00000675708.1:c.-196+5261C=	ENSP00000501654.1:n.-196+5261C=
ENST00000676445.1:c.-196+6161C=	ENSP00000502206.1:n.-196+6161C=
XM_017025514.2:c.60+5261C=	XP_016881003.1:n.60+5261C=