Canonical Allele Identifier: CA1867008263

Gene: GABBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98515427_98515428delinsCT , CM000671.2:g.98515427_98515428delinsCT	GRCh38
NC_000009.11:g.101277709_101277710delinsCT , CM000671.1:g.101277709_101277710delinsCT	GRCh37
NC_000009.10:g.100317530_100317531delinsCT	NCBI36
NG_016426.1:g.198770_198771delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000259455.4:c.631-18914_631-18913delinsAG MANE Select	ENSP00000259455.2:n.631-18914_631-18913de...
ENST00000637410.1:n.409-18914_409-18913delinsAG
ENST00000259455.3:c.631-18914_631-18913delinsAG	ENSP00000259455.2:n.631-18914_631-18913de...
ENST00000477471.1:n.418-18914_418-18913delinsAG
ENST00000634227.1:n.405-18914_405-18913delinsAG
ENST00000634919.1:n.306+566_306+567delinsAG
NM_005458.7:c.631-18914_631-18913delinsAG	NP_005449.5:n.631-18914_631-18913delinsAG...
XM_005252316.3:c.-144-18914_-144-18913delinsAG	XP_005252373.1:n.-144-18914_-144-18913del...
XM_005252316.5:c.-144-18914_-144-18913delinsAG	XP_005252373.1:n.-144-18914_-144-18913del...
XM_017015331.2:c.337-18914_337-18913delinsAG	XP_016870820.1:n.337-18914_337-18913delin...
NM_005458.8:c.631-18914_631-18913delinsAG MANE Select	NP_005449.5:n.631-18914_631-18913delinsAG...