Canonical Allele Identifier: CA1455320753

Gene: GABRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47407014_47407015delinsTA , CM000666.2:g.47407014_47407015delinsTA	GRCh38
NC_000004.11:g.47409031_47409032delinsTA , CM000666.1:g.47409031_47409032delinsTA	GRCh37
NC_000004.10:g.47103788_47103789delinsTA	NCBI36
NG_051831.1:g.380737_380738delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295454.8:c.1080+88_1080+89delinsTA MANE Select	ENSP00000295454.3:n.1080+88_1080+89delinsTA
ENST00000295454.7:c.1080+88_1080+89delinsTA	ENSP00000295454.3:n.1080+88_1080+89delinsTA
NM_000812.3:c.1080+88_1080+89delinsTA	NP_000803.2:n.1080+88_1080+89delinsTA
XM_011513678.1:c.1059+88_1059+89delinsTA	XP_011511980.1:n.1059+88_1059+89delinsTA
XM_017007985.1:c.429+88_429+89delinsTA	XP_016863474.1:n.429+88_429+89delinsTA
XM_024453976.1:c.981+88_981+89delinsTA	XP_024309744.1:n.981+88_981+89delinsTA
XM_024453977.1:c.981+88_981+89delinsTA	XP_024309745.1:n.981+88_981+89delinsTA
XM_024453978.1:c.981+88_981+89delinsTA	XP_024309746.1:n.981+88_981+89delinsTA
NM_000812.4:c.1080+88_1080+89delinsTA MANE Select	NP_000803.2:n.1080+88_1080+89delinsTA