Canonical Allele Identifier: CA297930312

Gene: CDH2

Linked Data

• dbSNP Id: rs879520389
• MyVariant Identifiers: chr18:g.25700793T>A (hg19) ; chr18:g.28120829T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.28120829T>A , CM000680.2:g.28120829T>A	GRCh38
NC_000018.9:g.25700793T>A , CM000680.1:g.25700793T>A	GRCh37
NC_000018.8:g.23954791T>A	NCBI36
NG_011959.1:g.61653A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000269141.8:c.172+26844A>T MANE Select	ENSP00000269141.3:n.172+26844A>T
ENST00000413878.2:c.-84+26844A>T	ENSP00000414269.2:n.-84+26844A>T
ENST00000430882.6:c.-275-23575A>T	ENSP00000412120.2:n.-275-23575A>T
ENST00000675708.1:c.-84+26844A>T	ENSP00000501654.1:n.-84+26844A>T
ENST00000676445.1:c.-84+26844A>T	ENSP00000502206.1:n.-84+26844A>T
ENST00000269141.7:c.172+26844A>T	ENSP00000269141.3:n.172+26844A>T
ENST00000413878.1:c.-84+26844A>T	ENSP00000414269.1:n.-84+26844A>T
NM_001792.3:c.172+26844A>T	NP_001783.2:n.172+26844A>T
NM_001792.4:c.172+26844A>T	NP_001783.2:n.172+26844A>T
XM_005258181.2:c.118+26844A>T	XP_005258238.1:n.118+26844A>T
XM_011525787.1:c.118+26844A>T	XP_011524089.1:n.118+26844A>T
XM_011525788.1:c.-84+26844A>T	XP_011524090.1:n.-84+26844A>T
XM_017025514.2:c.172+26844A>T	XP_016881003.1:n.172+26844A>T
NM_001792.5:c.172+26844A>T MANE Select	NP_001783.2:n.172+26844A>T