Canonical Allele Identifier: CA283273147

Gene: CDH1

Linked Data

• dbSNP Id: rs1006802286
• MyVariant Identifiers: chr16:g.68771202T>C (hg19) ; chr16:g.68737299T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68737299T>C , CM000678.2:g.68737299T>C	GRCh38
NC_000016.9:g.68771202T>C , CM000678.1:g.68771202T>C	GRCh37
NC_000016.8:g.67328703T>C	NCBI36
NG_008021.1:g.5008T>C , LRG_301:g.5008T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261769.10:c.-117T>C MANE Select	ENSP00000261769.4:n.-117T>C
ENST00000261769.9:c.-117T>C	ENSP00000261769.4:n.-117T>C
ENST00000611625.4:c.-117T>C	ENSP00000481063.1:n.-117T>C
ENST00000612417.4:c.-117T>C	ENSP00000478360.1:n.-117T>C
NM_004360.3:c.-117T>C , LRG_301t1:c.-117T>C	NP_004351.1:n.-117T>C
NM_001317184.1:c.-117T>C	NP_001304113.1:n.-117T>C
NM_001317185.1:c.-1732T>C	NP_001304114.1:n.-1732T>C
NM_001317186.1:c.-1936T>C	NP_001304115.1:n.-1936T>C
NM_004360.4:c.-117T>C	NP_004351.1:n.-117T>C
NM_004360.5:c.-117T>C MANE Select	NP_004351.1:n.-117T>C
NM_001317184.2:c.-117T>C	NP_001304113.1:n.-117T>C
NM_001317185.2:c.-1732T>C	NP_001304114.1:n.-1732T>C
NM_001317186.2:c.-1936T>C	NP_001304115.1:n.-1936T>C