Canonical Allele Identifier: CA623139867

Gene: CDH1

Linked Data

• dbSNP Id: rs1397744582
• gnomAD v2: 16-68771205-G-C
• gnomAD v3: 16-68737302-G-C
• gnomAD v4: 16-68737302-G-C
• MyVariant Identifiers: chr16:g.68771205G>C (hg19) ; chr16:g.68737302G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737302G>C , CM000678.2:g.68737302G>C	GRCh38
NC_000016.9:g.68771205G>C , CM000678.1:g.68771205G>C	GRCh37
NC_000016.8:g.67328706G>C	NCBI36
NG_008021.1:g.5011G>C , LRG_301:g.5011G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-114G>C MANE Select	ENSP00000261769.4:n.-114G>C
ENST00000261769.9:c.-114G>C	ENSP00000261769.4:n.-114G>C
ENST00000611625.4:c.-114G>C	ENSP00000481063.1:n.-114G>C
ENST00000612417.4:c.-114G>C	ENSP00000478360.1:n.-114G>C
NM_004360.3:c.-114G>C , LRG_301t1:c.-114G>C	NP_004351.1:n.-114G>C
NM_001317184.1:c.-114G>C	NP_001304113.1:n.-114G>C
NM_001317185.1:c.-1729G>C	NP_001304114.1:n.-1729G>C
NM_001317186.1:c.-1933G>C	NP_001304115.1:n.-1933G>C
NM_004360.4:c.-114G>C	NP_004351.1:n.-114G>C
NM_004360.5:c.-114G>C MANE Select	NP_004351.1:n.-114G>C
NM_001317184.2:c.-114G>C	NP_001304113.1:n.-114G>C
NM_001317185.2:c.-1729G>C	NP_001304114.1:n.-1729G>C
NM_001317186.2:c.-1933G>C	NP_001304115.1:n.-1933G>C