Canonical Allele Identifier: CA2428297156

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48523752A= , CM000685.2:g.48523752A=	GRCh38
NC_000023.10:g.48382140A= , CM000685.1:g.48382140A=	GRCh37
NC_000023.9:g.48267084A=	NCBI36
NG_007452.1:g.6977A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.-20A= MANE Select	ENSP00000417052.1:n.-20A=
ENST00000651615.1:c.-20A=	ENSP00000498524.1:n.-20A=
ENST00000276096.10:n.110-171A=
ENST00000414061.1:c.-20A=	ENSP00000405832.1:n.-20A=
ENST00000446158.5:c.-20A=	ENSP00000390031.1:n.-20A=
ENST00000495186.5:c.-20A=	ENSP00000417052.1:n.-20A=
ENST00000498425.1:n.104-2A=
NM_006579.2:c.-20A=	NP_006570.1:n.-20A=
NM_006579.3:c.-20A= MANE Select	NP_006570.1:n.-20A=