Canonical Allele Identifier: CA2428298216

Gene: EBP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48526990G= , CM000685.2:g.48526990G=	GRCh38
NC_000023.10:g.48385378G= , CM000685.1:g.48385378G=	GRCh37
NC_000023.9:g.48270322G=	NCBI36
NG_007452.1:g.10215G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495186.6:c.303G= MANE Select	ENSP00000417052.1:p.Trp101=
ENST00000651615.1:c.303G=	ENSP00000498524.1:p.Trp101=
ENST00000276096.10:n.261G=
ENST00000414061.1:c.303G=	ENSP00000405832.1:p.Trp101=
ENST00000446158.5:c.303G=	ENSP00000390031.1:p.Trp101=
ENST00000466461.1:n.142G=
ENST00000495186.5:c.303G=	ENSP00000417052.1:p.Trp101=
ENST00000498425.1:n.424G=
NM_006579.2:c.303G=	NP_006570.1:p.Trp101=
NM_006579.3:c.303G= MANE Select	NP_006570.1:p.Trp101=