Canonical Allele Identifier: CA396458069

Gene: CDH1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68808802T>C , CM000678.2:g.68808802T>C	GRCh38
NC_000016.9:g.68842705T>C , CM000678.1:g.68842705T>C	GRCh37
NC_000016.8:g.67400206T>C	NCBI36
NG_008021.1:g.76511T>C , LRG_301:g.76511T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.641T>C MANE Select	ENSP00000261769.4:p.Leu214Pro
ENST00000261769.9:c.641T>C	ENSP00000261769.4:p.Leu214Pro
ENST00000422392.6:c.641T>C	ENSP00000414946.2:p.Leu214Pro
ENST00000561751.1:c.408T>C
ENST00000562836.5:n.712T>C
ENST00000564676.5:n.923T>C
ENST00000566510.5:c.531+235T>C	ENSP00000458139.1:n.531+235T>C
ENST00000566612.5:c.641T>C	ENSP00000454782.1:p.Leu214Pro
ENST00000567320.1:n.151T>C
ENST00000611625.4:c.641T>C	ENSP00000481063.1:p.Leu214Pro
ENST00000612417.4:c.641T>C	ENSP00000478360.1:p.Leu214Pro
ENST00000621016.4:c.641T>C	ENSP00000480664.1:p.Leu214Pro
NM_004360.3:c.641T>C , LRG_301t1:c.641T>C	NP_004351.1:p.Leu214Pro
XM_011523488.1:c.-95T>C	XP_011521790.1:n.-95T>C
XM_011523489.1:c.-95T>C	XP_011521791.1:n.-95T>C
NM_001317184.1:c.641T>C	NP_001304113.1:p.Leu214Pro
NM_001317185.1:c.-975T>C	NP_001304114.1:n.-975T>C
NM_001317186.1:c.-1179T>C	NP_001304115.1:n.-1179T>C
NM_004360.4:c.641T>C	NP_004351.1:p.Leu214Pro
NM_004360.5:c.641T>C MANE Select	NP_004351.1:p.Leu214Pro
NM_001317184.2:c.641T>C	NP_001304113.1:p.Leu214Pro
NM_001317185.2:c.-975T>C	NP_001304114.1:n.-975T>C
NM_001317186.2:c.-1179T>C	NP_001304115.1:n.-1179T>C