Canonical Allele Identifier: CA2642690502

Gene: GABRD

Linked Data

• gnomAD v4: 1-2024553-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2024553G>T , CM000663.2:g.2024553G>T	GRCh38
NC_000001.10:g.1955992G>T , CM000663.1:g.1955992G>T	GRCh37
NC_000001.9:g.1945852G>T	NCBI36
NG_008168.1:g.10225G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.69-389G>T MANE Select	ENSP00000367848.4:n.69-389G>T
ENST00000638411.1:c.69-389G>T	ENSP00000491632.1:n.69-389G>T
ENST00000638604.1:n.133-389G>T
ENST00000638771.1:c.69-389G>T	ENSP00000492435.1:n.69-389G>T
ENST00000639045.1:c.*55-389G>T	ENSP00000491997.1:n.*55-389G>T
ENST00000639777.1:n.284G>T
ENST00000639935.1:n.106-389G>T
ENST00000640030.1:c.9-389G>T	ENSP00000491411.1:n.9-389G>T
ENST00000640067.1:c.69-389G>T	ENSP00000491844.1:n.69-389G>T
ENST00000640423.1:n.78-389G>T
ENST00000640949.1:c.69-389G>T	ENSP00000492500.1:n.69-389G>T
ENST00000378585.5:c.69-389G>T	ENSP00000367848.4:n.69-389G>T
NM_000815.4:c.69-389G>T	NP_000806.2:n.69-389G>T
XM_011541194.1:c.108-389G>T	XP_011539496.1:n.108-389G>T
XM_011541194.3:c.108-389G>T	XP_011539496.1:n.108-389G>T
XM_017000936.1:c.385G>T	XP_016856425.1:p.Val129Leu
NM_000815.5:c.69-389G>T MANE Select	NP_000806.2:n.69-389G>T