Canonical Allele Identifier: CA1455320766

Gene: GABRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47407021_47407022delinsAT , CM000666.2:g.47407021_47407022delinsAT	GRCh38
NC_000004.11:g.47409038_47409039delinsAT , CM000666.1:g.47409038_47409039delinsAT	GRCh37
NC_000004.10:g.47103795_47103796delinsAT	NCBI36
NG_051831.1:g.380744_380745delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295454.8:c.1080+95_1080+96delinsAT MANE Select	ENSP00000295454.3:n.1080+95_1080+96delinsAT
ENST00000295454.7:c.1080+95_1080+96delinsAT	ENSP00000295454.3:n.1080+95_1080+96delinsAT
NM_000812.3:c.1080+95_1080+96delinsAT	NP_000803.2:n.1080+95_1080+96delinsAT
XM_011513678.1:c.1059+95_1059+96delinsAT	XP_011511980.1:n.1059+95_1059+96delinsAT
XM_017007985.1:c.429+95_429+96delinsAT	XP_016863474.1:n.429+95_429+96delinsAT
XM_024453976.1:c.981+95_981+96delinsAT	XP_024309744.1:n.981+95_981+96delinsAT
XM_024453977.1:c.981+95_981+96delinsAT	XP_024309745.1:n.981+95_981+96delinsAT
XM_024453978.1:c.981+95_981+96delinsAT	XP_024309746.1:n.981+95_981+96delinsAT
NM_000812.4:c.1080+95_1080+96delinsAT MANE Select	NP_000803.2:n.1080+95_1080+96delinsAT