Canonical Allele Identifier: CA1866959750

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98380517_98380518delinsTC , CM000671.2:g.98380517_98380518delinsTC	GRCh38
NC_000009.11:g.101142799_101142800delinsTC , CM000671.1:g.101142799_101142800delinsTC	GRCh37
NC_000009.10:g.100182620_100182621delinsTC	NCBI36
NG_016426.1:g.333680_333681delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.1662+5122_1662+5123delinsGA MANE Select	ENSP00000259455.2:n.1662+5122_1662+5123de...
ENST00000637410.1:n.1440+5122_1440+5123delinsGA
ENST00000259455.3:c.1662+5122_1662+5123delinsGA	ENSP00000259455.2:n.1662+5122_1662+5123de...
ENST00000634314.1:n.167+5122_167+5123delinsGA
NM_005458.7:c.1662+5122_1662+5123delinsGA	NP_005449.5:n.1662+5122_1662+5123delinsGA...
XM_005252316.3:c.888+5122_888+5123delinsGA	XP_005252373.1:n.888+5122_888+5123delinsG...
XM_005252316.5:c.888+5122_888+5123delinsGA	XP_005252373.1:n.888+5122_888+5123delinsG...
XM_017015331.2:c.1368+5122_1368+5123delinsGA	XP_016870820.1:n.1368+5122_1368+5123delin...
XM_017015332.2:c.888+5122_888+5123delinsGA	XP_016870821.1:n.888+5122_888+5123delinsG...
NM_005458.8:c.1662+5122_1662+5123delinsGA MANE Select	NP_005449.5:n.1662+5122_1662+5123delinsGA...