Canonical Allele Identifier: CA730157586

Gene: GABRD

Linked Data

• dbSNP Id: rs1160143513
• gnomAD v3: 1-2024475-T-TC
• gnomAD v4: 1-2024475-T-TC
• MyVariant Identifiers: chr1:g.1955914_1955915insC (hg19) ; chr1:g.2024475_2024476insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024477dup , CM000663.2:g.2024477dup	GRCh38
NC_000001.10:g.1955916dup , CM000663.1:g.1955916dup	GRCh37
NC_000001.9:g.1945776dup	NCBI36
NG_008168.1:g.10149dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.69-465dup MANE Select	ENSP00000367848.4:n.69-465dup
ENST00000638411.1:c.69-465dup	ENSP00000491632.1:n.69-465dup
ENST00000638604.1:n.133-465dup
ENST00000638771.1:c.69-465dup	ENSP00000492435.1:n.69-465dup
ENST00000639045.1:c.*55-465dup	ENSP00000491997.1:n.*55-465dup
ENST00000639777.1:n.208dup
ENST00000639935.1:n.106-465dup
ENST00000640030.1:c.9-465dup	ENSP00000491411.1:n.9-465dup
ENST00000640067.1:c.69-465dup	ENSP00000491844.1:n.69-465dup
ENST00000640423.1:n.78-465dup
ENST00000640949.1:c.69-465dup	ENSP00000492500.1:n.69-465dup
ENST00000378585.5:c.69-465dup	ENSP00000367848.4:n.69-465dup
NM_000815.4:c.69-465dup	NP_000806.2:n.69-465dup
XM_011541194.1:c.108-465dup	XP_011539496.1:n.108-465dup
XM_011541194.3:c.108-465dup	XP_011539496.1:n.108-465dup
XM_017000936.1:c.309dup	XP_016856425.1:p.Ser104LeufsTer?
NM_000815.5:c.69-465dup MANE Select	NP_000806.2:n.69-465dup