Canonical Allele Identifier: CA1866927635

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98442760_98442761delinsAG , CM000671.2:g.98442760_98442761delinsAG	GRCh38
NC_000009.11:g.101205042_101205043delinsAG , CM000671.1:g.101205042_101205043delinsAG	GRCh37
NC_000009.10:g.100244863_100244864delinsAG	NCBI36
NG_016426.1:g.271437_271438delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1236+11220_1236+11221delinsCT MANE Select	ENSP00000259455.2:n.1236+11220_1236+11221delinsCT
ENST00000637410.1:n.1014+11220_1014+11221delinsCT
ENST00000259455.3:c.1236+11220_1236+11221delinsCT	ENSP00000259455.2:n.1236+11220_1236+11221delinsCT
NM_005458.7:c.1236+11220_1236+11221delinsCT	NP_005449.5:n.1236+11220_1236+11221delinsCT
XM_005252316.3:c.462+11220_462+11221delinsCT	XP_005252373.1:n.462+11220_462+11221delinsCT
XM_005252316.5:c.462+11220_462+11221delinsCT	XP_005252373.1:n.462+11220_462+11221delinsCT
XM_017015331.2:c.942+11220_942+11221delinsCT	XP_016870820.1:n.942+11220_942+11221delinsCT
XM_017015332.2:c.462+11220_462+11221delinsCT	XP_016870821.1:n.462+11220_462+11221delinsCT
NM_005458.8:c.1236+11220_1236+11221delinsCT MANE Select	NP_005449.5:n.1236+11220_1236+11221delinsCT