Canonical Allele Identifier: CA1600540394

Gene: GABRP

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.170813419A= , CM000667.2:g.170813419A=	GRCh38
NC_000005.9:g.170240423A= , CM000667.1:g.170240423A=	GRCh37
NC_000005.8:g.170173001A=	NCBI36
NG_052803.1:g.34701A=

Transcript Alleles

HGVS	Amino-acid Change
NM_014211.3:c.*1161A= MANE Select	NP_055026.1:n.*1161A=
ENST00000265294.9:c.*1161A= MANE Select	ENSP00000265294.4:n.*1161A=
NM_001291985.1:c.*1426A=	NP_001278914.1:n.*1426A=
NM_001291985.2:c.*1426A=	NP_001278914.1:n.*1426A=
NM_014211.2:c.*1161A=	NP_055026.1:n.*1161A=
ENST00000265294.8:c.*1161A=	ENSP00000265294.4:n.*1161A=
ENST00000518525.5:c.*1161A=	ENSP00000430100.1:n.*1161A=
XM_005265872.2:c.*1161A=	XP_005265929.1:n.*1161A=
XM_011534502.1:c.*1161A=	XP_011532804.1:n.*1161A=
XM_011534503.1:c.*1161A=	XP_011532805.1:n.*1161A=
XM_011534504.1:c.*1161A=	XP_011532806.1:n.*1161A=
XM_011534505.1:c.*1161A=	XP_011532807.1:n.*1161A=
XM_011534506.1:c.*1426A=	XP_011532808.1:n.*1426A=
XM_024446012.1:c.*1161A=	XP_024301780.1:n.*1161A=