Canonical Allele Identifier: CA1866959561
Gene: GABBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.98380359_98380362delinsCCCT , CM000671.2:g.98380359_98380362delinsCCCT GRCh38
NC_000009.11:g.101142641_101142644delinsCCCT , CM000671.1:g.101142641_101142644delinsCCCT GRCh37
NC_000009.10:g.100182462_100182465delinsCCCT NCBI36
NG_016426.1:g.333836_333839delinsAGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000259455.4:c.1662+5278_1662+5281delinsAGGG MANE Select ENSP00000259455.2:n.1662+5278_1662+5281de...
ENST00000637410.1:n.1440+5278_1440+5281delinsAGGG
ENST00000259455.3:c.1662+5278_1662+5281delinsAGGG ENSP00000259455.2:n.1662+5278_1662+5281de...
ENST00000634314.1:n.167+5278_167+5281delinsAGGG
NM_005458.7:c.1662+5278_1662+5281delinsAGGG NP_005449.5:n.1662+5278_1662+5281delinsAG...
XM_005252316.3:c.888+5278_888+5281delinsAGGG XP_005252373.1:n.888+5278_888+5281delinsA...
XM_005252316.5:c.888+5278_888+5281delinsAGGG XP_005252373.1:n.888+5278_888+5281delinsA...
XM_017015331.2:c.1368+5278_1368+5281delinsAGGG XP_016870820.1:n.1368+5278_1368+5281delin...
XM_017015332.2:c.888+5278_888+5281delinsAGGG XP_016870821.1:n.888+5278_888+5281delinsA...
NM_005458.8:c.1662+5278_1662+5281delinsAGGG MANE Select NP_005449.5:n.1662+5278_1662+5281delinsAG...