Canonical Allele Identifier: CA1866959793

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98380568_98380574delinsCTCCACG , CM000671.2:g.98380568_98380574delinsCTCCACG	GRCh38
NC_000009.11:g.101142850_101142856delinsCTCCACG , CM000671.1:g.101142850_101142856delinsCTCCACG	GRCh37
NC_000009.10:g.100182671_100182677delinsCTCCACG	NCBI36
NG_016426.1:g.333624_333630delinsCGTGGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1662+5066_1662+5072delinsCGTGGAG MANE Select	ENSP00000259455.2:n.1662+5066_1662+5072delinsCGTGGAG
ENST00000637410.1:n.1440+5066_1440+5072delinsCGTGGAG
ENST00000259455.3:c.1662+5066_1662+5072delinsCGTGGAG	ENSP00000259455.2:n.1662+5066_1662+5072delinsCGTGGAG
ENST00000634314.1:n.167+5066_167+5072delinsCGTGGAG
NM_005458.7:c.1662+5066_1662+5072delinsCGTGGAG	NP_005449.5:n.1662+5066_1662+5072delinsCGTGGAG
XM_005252316.3:c.888+5066_888+5072delinsCGTGGAG	XP_005252373.1:n.888+5066_888+5072delinsCGTGGAG
XM_005252316.5:c.888+5066_888+5072delinsCGTGGAG	XP_005252373.1:n.888+5066_888+5072delinsCGTGGAG
XM_017015331.2:c.1368+5066_1368+5072delinsCGTGGAG	XP_016870820.1:n.1368+5066_1368+5072delinsCGTGGAG
XM_017015332.2:c.888+5066_888+5072delinsCGTGGAG	XP_016870821.1:n.888+5066_888+5072delinsCGTGGAG
NM_005458.8:c.1662+5066_1662+5072delinsCGTGGAG MANE Select	NP_005449.5:n.1662+5066_1662+5072delinsCGTGGAG