Canonical Allele Identifier: CA396451378

Gene: CDH1

Linked Data

• ClinVar Variation Id: 1485142
• ClinVar RCV Id: RCV002008436
• dbSNP Id: rs1191249318
• gnomAD v2: 16-68771353-T-C
• gnomAD v4: 16-68737450-T-C
• MyVariant Identifiers: chr16:g.68771353T>C (hg19) ; chr16:g.68737450T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737450T>C , CM000678.2:g.68737450T>C	GRCh38
NC_000016.9:g.68771353T>C , CM000678.1:g.68771353T>C	GRCh37
NC_000016.8:g.67328854T>C	NCBI36
NG_008021.1:g.5159T>C , LRG_301:g.5159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.35T>C MANE Select	ENSP00000261769.4:p.Leu12Pro
ENST00000261769.9:c.35T>C	ENSP00000261769.4:p.Leu12Pro
ENST00000422392.6:c.35T>C	ENSP00000414946.2:p.Leu12Pro
ENST00000566510.5:c.35T>C	ENSP00000458139.1:p.Leu12Pro
ENST00000566612.5:c.35T>C	ENSP00000454782.1:p.Leu12Pro
ENST00000611625.4:c.35T>C	ENSP00000481063.1:p.Leu12Pro
ENST00000612417.4:c.35T>C	ENSP00000478360.1:p.Leu12Pro
ENST00000621016.4:c.35T>C	ENSP00000480664.1:p.Leu12Pro
NM_004360.3:c.35T>C , LRG_301t1:c.35T>C	NP_004351.1:p.Leu12Pro
NM_001317184.1:c.35T>C	NP_001304113.1:p.Leu12Pro
NM_001317185.1:c.-1581T>C	NP_001304114.1:n.-1581T>C
NM_001317186.1:c.-1785T>C	NP_001304115.1:n.-1785T>C
NM_004360.4:c.35T>C	NP_004351.1:p.Leu12Pro
NM_004360.5:c.35T>C MANE Select	NP_004351.1:p.Leu12Pro
NM_001317184.2:c.35T>C	NP_001304113.1:p.Leu12Pro
NM_001317185.2:c.-1581T>C	NP_001304114.1:n.-1581T>C
NM_001317186.2:c.-1785T>C	NP_001304115.1:n.-1785T>C