Canonical Allele Identifier: CA2166933129

Gene: ENTREP2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.29132557T= , CM000677.2:g.29132557T=	GRCh38
NC_000015.9:g.29424760T= , CM000677.1:g.29424760T=	GRCh37
NC_000015.8:g.27212052T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261275.5:c.928-3693A= MANE Select	ENSP00000261275.4:n.928-3693A=
ENST00000261275.4:c.928-3693A=	ENSP00000261275.4:n.928-3693A=
ENST00000560021.1:n.664-3693A=
NM_015307.1:c.928-3693A=	NP_056122.1:n.928-3693A=
XM_011521407.1:c.1039-3693A=	XP_011519709.1:n.1039-3693A=
XM_011521407.2:c.1039-3693A=	XP_011519709.1:n.1039-3693A=
NM_001387214.1:c.793-3693A=	NP_001374143.1:n.793-3693A=
NM_001387215.1:c.640-3693A=	NP_001374144.1:n.640-3693A=
NM_001387216.1:c.640-3693A=	NP_001374145.1:n.640-3693A=
NM_001387217.1:c.505-3693A=	NP_001374146.1:n.505-3693A=
NM_015307.2:c.928-3693A= MANE Select	NP_056122.1:n.928-3693A=