Canonical Allele Identifier: CA2576960568

Gene: EPCAM

Linked Data

• gnomAD v4: 2-47377152-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47377153_47377154insAA , CM000664.2:g.47377153_47377154insAA	GRCh38
NC_000002.11:g.47604292_47604293insAA , CM000664.1:g.47604292_47604293insAA	GRCh37
NC_000002.10:g.47457796_47457797insAA	NCBI36
NG_012352.2:g.36991_36992insAA , LRG_215:g.36991_36992insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263735.9:c.555+76_555+77insAA MANE Select	ENSP00000263735.4:n.555+76_555+77insAA
ENST00000263735.8:c.555+76_555+77insAA	ENSP00000263735.4:n.555+76_555+77insAA
ENST00000405271.5:c.639+76_639+77insAA	ENSP00000385476.1:n.639+76_639+77insAA
ENST00000456133.5:c.639+76_639+77insAA	ENSP00000410675.1:n.639+76_639+77insAA
ENST00000490733.1:n.404+76_404+77insAA
NM_002354.2:c.555+76_555+77insAA , LRG_215t1:c.555+76_555+77insAA	NP_002345.2:n.555+76_555+77insAA
NM_002354.3:c.555+76_555+77insAA MANE Select	NP_002345.2:n.555+76_555+77insAA