Canonical Allele Identifier: CA2738465538

Gene: EBP

Linked Data

• dbSNP Id: rs2147156445

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48527136del , CM000685.2:g.48527136del	GRCh38
NC_000023.10:g.48385524del , CM000685.1:g.48385524del	GRCh37
NC_000023.9:g.48270468del	NCBI36
NG_007452.1:g.10361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.339-19del MANE Select	ENSP00000417052.1:n.339-19del
ENST00000651615.1:c.339-19del	ENSP00000498524.1:n.339-19del
ENST00000276096.10:n.297-19del
ENST00000414061.1:c.339-19del	ENSP00000405832.1:n.339-19del
ENST00000446158.5:c.339-19del	ENSP00000390031.1:n.339-19del
ENST00000466461.1:n.178-19del
ENST00000495186.5:c.339-19del	ENSP00000417052.1:n.339-19del
ENST00000498425.1:n.460-19del
NM_006579.2:c.339-19del	NP_006570.1:n.339-19del
NM_006579.3:c.339-19del MANE Select	NP_006570.1:n.339-19del