Canonical Allele Identifier: CA1141741307

Gene: GABRD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.2025064_2025065delinsGG , CM000663.2:g.2025064_2025065delinsGG	GRCh38
NC_000001.10:g.1956503_1956504delinsGG , CM000663.1:g.1956503_1956504delinsGG	GRCh37
NC_000001.9:g.1946363_1946364delinsGG	NCBI36
NG_008168.1:g.10736_10737delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378585.7:c.181+10_181+11delinsGG MANE Select	ENSP00000367848.4:n.181+10_181+11delinsGG
ENST00000638411.1:c.181+10_181+11delinsGG	ENSP00000491632.1:n.181+10_181+11delinsGG
ENST00000638604.1:n.245+10_245+11delinsGG
ENST00000638771.1:c.181+10_181+11delinsGG	ENSP00000492435.1:n.181+10_181+11delinsGG
ENST00000639045.1:c.*167+10_*167+11delinsGG	ENSP00000491997.1:n.*167+10_*167+11delinsGG
ENST00000639777.1:n.785+10_785+11delinsGG
ENST00000639935.1:n.218+10_218+11delinsGG
ENST00000640030.1:c.121+10_121+11delinsGG	ENSP00000491411.1:n.121+10_121+11delinsGG
ENST00000640067.1:c.181+10_181+11delinsGG	ENSP00000491844.1:n.181+10_181+11delinsGG
ENST00000640423.1:n.190+10_190+11delinsGG
ENST00000640949.1:c.181+10_181+11delinsGG	ENSP00000492500.1:n.181+10_181+11delinsGG
ENST00000378585.5:c.181+10_181+11delinsGG	ENSP00000367848.4:n.181+10_181+11delinsGG
NM_000815.4:c.181+10_181+11delinsGG	NP_000806.2:n.181+10_181+11delinsGG
XM_011541194.1:c.220+10_220+11delinsGG	XP_011539496.1:n.220+10_220+11delinsGG
XM_011541194.3:c.220+10_220+11delinsGG	XP_011539496.1:n.220+10_220+11delinsGG
XM_017000936.1:c.886+10_886+11delinsGG	XP_016856425.1:n.886+10_886+11delinsGG
NM_000815.5:c.181+10_181+11delinsGG MANE Select	NP_000806.2:n.181+10_181+11delinsGG