Canonical Allele Identifier: CA2465842330

Gene: GABRE

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151969635C= , CM000685.2:g.151969635C=	GRCh38
NC_000023.10:g.151138107C= , CM000685.1:g.151138107C=	GRCh37
NC_000023.9:g.150888763C=	NCBI36
NG_012511.1:g.10045G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370328.4:c.342+34G= MANE Select	ENSP00000359353.3:n.342+34G=
ENST00000370328.3:c.342+34G=	ENSP00000359353.3:n.342+34G=
ENST00000441219.5:c.*388+34G=	ENSP00000389384.1:n.*388+34G=
ENST00000465405.1:n.470G=
ENST00000474932.1:n.68+34G=
NM_004961.3:c.342+34G=	NP_004952.2:n.342+34G=
XM_006724813.2:c.342+34G=	XP_006724876.2:n.342+34G=
XM_011531135.1:c.3+34G=	XP_011529437.1:n.3+34G=
XM_011531136.1:c.3+34G=	XP_011529438.1:n.3+34G=
XM_011531137.1:c.342+34G=	XP_011529439.1:n.342+34G=
XM_011531138.1:c.342+34G=	XP_011529440.1:n.342+34G=
XM_011531139.1:c.342+34G=	XP_011529441.1:n.342+34G=
XM_017029387.2:c.3+34G=	XP_016884876.1:n.3+34G=
XM_017029389.2:c.3+34G=	XP_016884878.1:n.3+34G=
XM_024452360.1:c.3+34G=	XP_024308128.1:n.3+34G=
NM_004961.4:c.342+34G= MANE Select	NP_004952.2:n.342+34G=