Canonical Allele Identifier: CA346723961

Gene: EPCAM

Linked Data

• dbSNP Id: rs2103753305
• MyVariant Identifiers: chr2:g.47604163A>T (hg19) ; chr2:g.47377024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47377024A>T , CM000664.2:g.47377024A>T	GRCh38
NC_000002.11:g.47604163A>T , CM000664.1:g.47604163A>T	GRCh37
NC_000002.10:g.47457667A>T	NCBI36
NG_012352.2:g.36862A>T , LRG_215:g.36862A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000263735.9:c.502A>T MANE Select	ENSP00000263735.4:p.Lys168Ter
ENST00000263735.8:c.502A>T	ENSP00000263735.4:p.Lys168Ter
ENST00000405271.5:c.586A>T	ENSP00000385476.1:p.Lys196Ter
ENST00000456133.5:c.586A>T	ENSP00000410675.1:p.Lys196Ter
ENST00000490733.1:n.351A>T
NM_002354.2:c.502A>T , LRG_215t1:c.502A>T	NP_002345.2:p.Lys168Ter
NM_002354.3:c.502A>T MANE Select	NP_002345.2:p.Lys168Ter