Canonical Allele Identifier: CA1866927747

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98442889_98442891delinsCCT , CM000671.2:g.98442889_98442891delinsCCT	GRCh38
NC_000009.11:g.101205171_101205173delinsCCT , CM000671.1:g.101205171_101205173delinsCCT	GRCh37
NC_000009.10:g.100244992_100244994delinsCCT	NCBI36
NG_016426.1:g.271307_271309delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1236+11090_1236+11092delinsAGG MANE Select	ENSP00000259455.2:n.1236+11090_1236+11092delinsAGG
ENST00000637410.1:n.1014+11090_1014+11092delinsAGG
ENST00000259455.3:c.1236+11090_1236+11092delinsAGG	ENSP00000259455.2:n.1236+11090_1236+11092delinsAGG
NM_005458.7:c.1236+11090_1236+11092delinsAGG	NP_005449.5:n.1236+11090_1236+11092delinsAGG
XM_005252316.3:c.462+11090_462+11092delinsAGG	XP_005252373.1:n.462+11090_462+11092delinsAGG
XM_005252316.5:c.462+11090_462+11092delinsAGG	XP_005252373.1:n.462+11090_462+11092delinsAGG
XM_017015331.2:c.942+11090_942+11092delinsAGG	XP_016870820.1:n.942+11090_942+11092delinsAGG
XM_017015332.2:c.462+11090_462+11092delinsAGG	XP_016870821.1:n.462+11090_462+11092delinsAGG
NM_005458.8:c.1236+11090_1236+11092delinsAGG MANE Select	NP_005449.5:n.1236+11090_1236+11092delinsAGG