Canonical Allele Identifier: CA1149429405

Gene: GABRD

Linked Data

• dbSNP Id: rs1658865205

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024480_2024482del , CM000663.2:g.2024480_2024482del	GRCh38
NC_000001.10:g.1955919_1955921del , CM000663.1:g.1955919_1955921del	GRCh37
NC_000001.9:g.1945779_1945781del	NCBI36
NG_008168.1:g.10152_10154del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.69-462_69-460del MANE Select	ENSP00000367848.4:n.69-462_69-460del
ENST00000638411.1:c.69-462_69-460del	ENSP00000491632.1:n.69-462_69-460del
ENST00000638604.1:n.133-462_133-460del
ENST00000638771.1:c.69-462_69-460del	ENSP00000492435.1:n.69-462_69-460del
ENST00000639045.1:c.*55-462_*55-460del	ENSP00000491997.1:n.*55-462_*55-460del
ENST00000639777.1:n.211_213del
ENST00000639935.1:n.106-462_106-460del
ENST00000640030.1:c.9-462_9-460del	ENSP00000491411.1:n.9-462_9-460del
ENST00000640067.1:c.69-462_69-460del	ENSP00000491844.1:n.69-462_69-460del
ENST00000640423.1:n.78-462_78-460del
ENST00000640949.1:c.69-462_69-460del	ENSP00000492500.1:n.69-462_69-460del
ENST00000378585.5:c.69-462_69-460del	ENSP00000367848.4:n.69-462_69-460del
NM_000815.4:c.69-462_69-460del	NP_000806.2:n.69-462_69-460del
XM_011541194.1:c.108-462_108-460del	XP_011539496.1:n.108-462_108-460del
XM_011541194.3:c.108-462_108-460del	XP_011539496.1:n.108-462_108-460del
XM_017000936.1:c.312_314del	XP_016856425.1:p.Ser105del
NM_000815.5:c.69-462_69-460del MANE Select	NP_000806.2:n.69-462_69-460del