Canonical Allele Identifier: CA2229948531

Gene: CDH1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68815584_68815586delinsGTC , CM000678.2:g.68815584_68815586delinsGTC	GRCh38
NC_000016.9:g.68849487_68849489delinsGTC , CM000678.1:g.68849487_68849489delinsGTC	GRCh37
NC_000016.8:g.67406988_67406990delinsGTC	NCBI36
NG_008021.1:g.83293_83295delinsGTC , LRG_301:g.83293_83295delinsGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.1390_1392delinsGTC MANE Select	ENSP00000261769.4:p.Val464=
ENST00000261769.9:c.1390_1392delinsGTC	ENSP00000261769.4:p.Val464=
ENST00000422392.6:c.1207_1209delinsGTC	ENSP00000414946.2:p.Val403=
ENST00000562836.5:n.1461_1463delinsGTC
ENST00000566510.5:c.*56_*58delinsGTC	ENSP00000458139.1:n.*56_*58delinsGTC
ENST00000566612.5:c.1390_1392delinsGTC	ENSP00000454782.1:p.Val464=
ENST00000611625.4:c.1453_1455delinsGTC	ENSP00000481063.1:p.Val485=
ENST00000612417.4:c.1390_1392delinsGTC	ENSP00000478360.1:p.Val464=
ENST00000621016.4:c.1390_1392delinsGTC	ENSP00000480664.1:p.Val464=
NM_004360.3:c.1390_1392delinsGTC , LRG_301t1:c.1390_1392delinsGTC	NP_004351.1:p.Val464=
XM_011523488.1:c.655_657delinsGTC	XP_011521790.1:p.Val219=
XM_011523489.1:c.655_657delinsGTC	XP_011521791.1:p.Val219=
NM_001317184.1:c.1207_1209delinsGTC	NP_001304113.1:p.Val403=
NM_001317185.1:c.-159_-157delinsGTC	NP_001304114.1:n.-159_-157delinsGTC
NM_001317186.1:c.-430_-428delinsGTC	NP_001304115.1:n.-430_-428delinsGTC
NM_004360.4:c.1390_1392delinsGTC	NP_004351.1:p.Val464=
NM_004360.5:c.1390_1392delinsGTC MANE Select	NP_004351.1:p.Val464=
NM_001317184.2:c.1207_1209delinsGTC	NP_001304113.1:p.Val403=
NM_001317185.2:c.-159_-157delinsGTC	NP_001304114.1:n.-159_-157delinsGTC
NM_001317186.2:c.-430_-428delinsGTC	NP_001304115.1:n.-430_-428delinsGTC