Canonical Allele Identifier: CA1866993878
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98541602_98541615delinsGCCACTGAGGGAAT , CM000671.2:g.98541602_98541615delinsGCCACTGAGGGAAT GRCh38
NC_000009.11:g.101303884_101303897delinsGCCACTGAGGGAAT , CM000671.1:g.101303884_101303897delinsGCCACTGAGGGAAT GRCh37
NC_000009.10:g.100343705_100343718delinsGCCACTGAGGGAAT NCBI36
NG_016426.1:g.172583_172596delinsATTCCCTCAGTGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000259455.4:c.630+258_630+271delinsATTCCCTCAGTGGC MANE Select ENSP00000259455.2:n.630+258_630+271delinsATTCCCTCAGTGGC
ENST00000637410.1:n.408+258_408+271delinsATTCCCTCAGTGGC
ENST00000259455.3:c.630+258_630+271delinsATTCCCTCAGTGGC ENSP00000259455.2:n.630+258_630+271delinsATTCCCTCAGTGGC
ENST00000477471.1:n.417+258_417+271delinsATTCCCTCAGTGGC
ENST00000634227.1:n.404+258_404+271delinsATTCCCTCAGTGGC
NM_005458.7:c.630+258_630+271delinsATTCCCTCAGTGGC NP_005449.5:n.630+258_630+271delinsATTCCCTCAGTGGC
XM_017015331.2:c.336+258_336+271delinsATTCCCTCAGTGGC XP_016870820.1:n.336+258_336+271delinsATTCCCTCAGTGGC
NM_005458.8:c.630+258_630+271delinsATTCCCTCAGTGGC MANE Select NP_005449.5:n.630+258_630+271delinsATTCCCTCAGTGGC