Canonical Allele Identifier: CA1149430029

Gene: GABRD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024970G= , CM000663.2:g.2024970G=	GRCh38
NC_000001.10:g.1956409G= , CM000663.1:g.1956409G=	GRCh37
NC_000001.9:g.1946269G=	NCBI36
NG_008168.1:g.10642G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.97G= MANE Select	ENSP00000367848.4:p.Gly33=
ENST00000638411.1:c.97G=	ENSP00000491632.1:p.Gly33=
ENST00000638604.1:n.161G=
ENST00000638771.1:c.97G=	ENSP00000492435.1:p.Gly33=
ENST00000639045.1:c.*83G=	ENSP00000491997.1:n.*83G=
ENST00000639777.1:n.701G=
ENST00000639935.1:n.134G=
ENST00000640030.1:c.37G=	ENSP00000491411.1:p.Gly13=
ENST00000640067.1:c.97G=	ENSP00000491844.1:p.Gly33=
ENST00000640423.1:n.106G=
ENST00000640949.1:c.97G=	ENSP00000492500.1:p.Gly33=
ENST00000378585.5:c.97G=	ENSP00000367848.4:p.Gly33=
NM_000815.4:c.97G=	NP_000806.2:p.Gly33=
XM_011541194.1:c.136G=	XP_011539496.1:p.Gly46=
XM_011541194.3:c.136G=	XP_011539496.1:p.Gly46=
XM_017000936.1:c.802G=	XP_016856425.1:p.Gly268=
NM_000815.5:c.97G= MANE Select	NP_000806.2:p.Gly33=