Canonical Allele Identifier: CA402100992

Gene: CDH2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.27952200G>A , CM000680.2:g.27952200G>A	GRCh38
NC_000018.9:g.25532164G>A , CM000680.1:g.25532164G>A	GRCh37
NC_000018.8:g.23786162G>A	NCBI36
NG_011959.1:g.230282C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001792.5:c.2674C>T MANE Select	NP_001783.2:p.Pro892Ser
ENST00000269141.8:c.2674C>T MANE Select	ENSP00000269141.3:p.Pro892Ser
NM_001308176.1:c.2581C>T	NP_001295105.1:p.Pro861Ser
NM_001308176.2:c.2581C>T	NP_001295105.1:p.Pro861Ser
NM_001792.3:c.2674C>T	NP_001783.2:p.Pro892Ser
NM_001792.4:c.2674C>T	NP_001783.2:p.Pro892Ser
ENST00000269141.7:c.2674C>T	ENSP00000269141.3:p.Pro892Ser
ENST00000399380.7:c.2581C>T	ENSP00000382312.3:p.Pro861Ser
ENST00000430882.6:c.2419C>T	ENSP00000412120.2:p.Pro807Ser
ENST00000674998.1:n.2639C>T
ENST00000675173.1:c.1151+11157C>T
ENST00000675688.1:c.466+11157C>T
ENST00000675708.1:c.*989C>T	ENSP00000501654.1:n.*989C>T
ENST00000676445.1:c.2419C>T	ENSP00000502206.1:p.Pro807Ser
XM_005258181.2:c.2620C>T	XP_005258238.1:p.Pro874Ser
XM_011525787.1:c.2460+11157C>T	XP_011524089.1:n.2460+11157C>T
XM_011525788.1:c.2419C>T	XP_011524090.1:p.Pro807Ser
XM_017025514.2:c.2514+11157C>T	XP_016881003.1:n.2514+11157C>T