Canonical Allele Identifier: CA2229953305

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68796548_68796551delinsCTGA , CM000678.2:g.68796548_68796551delinsCTGA	GRCh38
NC_000016.9:g.68830451_68830454delinsCTGA , CM000678.1:g.68830451_68830454delinsCTGA	GRCh37
NC_000016.8:g.67387952_67387955delinsCTGA	NCBI36
NG_008021.1:g.64257_64260delinsCTGA , LRG_301:g.64257_64260delinsCTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.164-5122_164-5119delinsCTGA MANE Select	ENSP00000261769.4:n.164-5122_164-5119delinsCTGA
ENST00000261769.9:c.164-5122_164-5119delinsCTGA	ENSP00000261769.4:n.164-5122_164-5119delinsCTGA
ENST00000422392.6:c.164-5122_164-5119delinsCTGA	ENSP00000414946.2:n.164-5122_164-5119delinsCTGA
ENST00000562836.5:n.235-5122_235-5119delinsCTGA
ENST00000564676.5:n.446-5122_446-5119delinsCTGA
ENST00000564745.1:n.159-5122_159-5119delinsCTGA
ENST00000566510.5:c.164-5122_164-5119delinsCTGA	ENSP00000458139.1:n.164-5122_164-5119delinsCTGA
ENST00000566612.5:c.164-5122_164-5119delinsCTGA	ENSP00000454782.1:n.164-5122_164-5119delinsCTGA
ENST00000611625.4:c.164-5122_164-5119delinsCTGA	ENSP00000481063.1:n.164-5122_164-5119delinsCTGA
ENST00000612417.4:c.164-5122_164-5119delinsCTGA	ENSP00000478360.1:n.164-5122_164-5119delinsCTGA
ENST00000621016.4:c.164-5122_164-5119delinsCTGA	ENSP00000480664.1:n.164-5122_164-5119delinsCTGA
NM_004360.3:c.164-5122_164-5119delinsCTGA , LRG_301t1:c.164-5122_164-5119delinsCTGA	NP_004351.1:n.164-5122_164-5119delinsCTGA
XM_011523488.1:c.-572-5122_-572-5119delinsCTGA	XP_011521790.1:n.-572-5122_-572-5119delinsCTGA
XM_011523489.1:c.-572-5122_-572-5119delinsCTGA	XP_011521791.1:n.-572-5122_-572-5119delinsCTGA
NM_001317184.1:c.164-5122_164-5119delinsCTGA	NP_001304113.1:n.164-5122_164-5119delinsCTGA
NM_001317185.1:c.-1452-5122_-1452-5119delinsCTGA	NP_001304114.1:n.-1452-5122_-1452-5119delinsCTGA
NM_001317186.1:c.-1656-5122_-1656-5119delinsCTGA	NP_001304115.1:n.-1656-5122_-1656-5119delinsCTGA
NM_004360.4:c.164-5122_164-5119delinsCTGA	NP_004351.1:n.164-5122_164-5119delinsCTGA
NM_004360.5:c.164-5122_164-5119delinsCTGA MANE Select	NP_004351.1:n.164-5122_164-5119delinsCTGA
NM_001317184.2:c.164-5122_164-5119delinsCTGA	NP_001304113.1:n.164-5122_164-5119delinsCTGA
NM_001317185.2:c.-1452-5122_-1452-5119delinsCTGA	NP_001304114.1:n.-1452-5122_-1452-5119delinsCTGA
NM_001317186.2:c.-1656-5122_-1656-5119delinsCTGA	NP_001304115.1:n.-1656-5122_-1656-5119delinsCTGA