Canonical Allele Identifier: CA1867008136

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98515301_98515302delinsCT , CM000671.2:g.98515301_98515302delinsCT	GRCh38
NC_000009.11:g.101277583_101277584delinsCT , CM000671.1:g.101277583_101277584delinsCT	GRCh37
NC_000009.10:g.100317404_100317405delinsCT	NCBI36
NG_016426.1:g.198896_198897delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259455.4:c.631-18788_631-18787delinsAG MANE Select	ENSP00000259455.2:n.631-18788_631-18787delinsAG
ENST00000637410.1:n.409-18788_409-18787delinsAG
ENST00000259455.3:c.631-18788_631-18787delinsAG	ENSP00000259455.2:n.631-18788_631-18787delinsAG
ENST00000477471.1:n.418-18788_418-18787delinsAG
ENST00000634227.1:n.405-18788_405-18787delinsAG
ENST00000634919.1:n.306+692_306+693delinsAG
NM_005458.7:c.631-18788_631-18787delinsAG	NP_005449.5:n.631-18788_631-18787delinsAG
XM_005252316.3:c.-144-18788_-144-18787delinsAG	XP_005252373.1:n.-144-18788_-144-18787delinsAG
XM_005252316.5:c.-144-18788_-144-18787delinsAG	XP_005252373.1:n.-144-18788_-144-18787delinsAG
XM_017015331.2:c.337-18788_337-18787delinsAG	XP_016870820.1:n.337-18788_337-18787delinsAG
NM_005458.8:c.631-18788_631-18787delinsAG MANE Select	NP_005449.5:n.631-18788_631-18787delinsAG