Canonical Allele Identifier: CA396472577

Gene: CDH1

Linked Data

• MyVariant Identifiers: chr16:g.68867338T>C (hg19) ; chr16:g.68833435T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.68833435T>C , CM000678.2:g.68833435T>C	GRCh38
NC_000016.9:g.68867338T>C , CM000678.1:g.68867338T>C	GRCh37
NC_000016.8:g.67424839T>C	NCBI36
NG_008021.1:g.101144T>C , LRG_301:g.101144T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261769.10:c.2585T>C MANE Select	ENSP00000261769.4:p.Leu862Ser
ENST00000261769.9:c.2585T>C	ENSP00000261769.4:p.Leu862Ser
ENST00000422392.6:c.2402T>C	ENSP00000414946.2:p.Leu801Ser
ENST00000562118.1:n.803T>C
ENST00000562836.5:n.2656T>C
ENST00000566510.5:c.*1251T>C	ENSP00000458139.1:n.*1251T>C
ENST00000566612.5:c.*825T>C	ENSP00000454782.1:n.*825T>C
ENST00000611625.4:c.2648T>C	ENSP00000481063.1:p.Leu883Ser
ENST00000612417.4:c.1854-756T>C	ENSP00000478360.1:n.1854-756T>C
ENST00000621016.4:c.1866-768T>C	ENSP00000480664.1:n.1866-768T>C
NM_004360.3:c.2585T>C , LRG_301t1:c.2585T>C	NP_004351.1:p.Leu862Ser
XM_011523488.1:c.1850T>C	XP_011521790.1:p.Leu617Ser
XM_011523489.1:c.1850T>C	XP_011521791.1:p.Leu617Ser
NM_001317184.1:c.2402T>C	NP_001304113.1:p.Leu801Ser
NM_001317185.1:c.1037T>C	NP_001304114.1:p.Leu346Ser
NM_001317186.1:c.620T>C	NP_001304115.1:p.Leu207Ser
NM_004360.4:c.2585T>C	NP_004351.1:p.Leu862Ser
NM_004360.5:c.2585T>C MANE Select	NP_004351.1:p.Leu862Ser
NM_001317184.2:c.2402T>C	NP_001304113.1:p.Leu801Ser
NM_001317185.2:c.1037T>C	NP_001304114.1:p.Leu346Ser
NM_001317186.2:c.620T>C	NP_001304115.1:p.Leu207Ser