Canonical Allele Identifier: CA769444387
Gene: EPCAM HGNC NCBI

Linked Data

dbSNP Id: rs1553343414
MyVariant Identifiers: chr2:g.47604368_47604369insTATT (hg19) chr2:g.47377229_47377230insTATT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47377230_47377231insATTT , CM000664.2:g.47377230_47377231insATTT GRCh38
NC_000002.11:g.47604369_47604370insATTT , CM000664.1:g.47604369_47604370insATTT GRCh37
NC_000002.10:g.47457873_47457874insATTT NCBI36
NG_012352.2:g.37068_37069insATTT , LRG_215:g.37068_37069insATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000263735.9:c.555+153_555+154insATTT MANE Select ENSP00000263735.4:n.555+153_555+154insATTT
ENST00000263735.8:c.555+153_555+154insATTT ENSP00000263735.4:n.555+153_555+154insATTT
ENST00000405271.5:c.639+153_639+154insATTT ENSP00000385476.1:n.639+153_639+154insATTT
ENST00000456133.5:c.639+153_639+154insATTT ENSP00000410675.1:n.639+153_639+154insATTT
ENST00000490733.1:n.404+153_404+154insATTT
NM_002354.2:c.555+153_555+154insATTT , LRG_215t1:c.555+153_555+154insATTT NP_002345.2:n.555+153_555+154insATTT
NM_002354.3:c.555+153_555+154insATTT MANE Select NP_002345.2:n.555+153_555+154insATTT
Search 100 bp 5'
Search 100 bp 3'