Canonical Allele Identifier: CA789596800
Gene: GLRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157078048del , CM000666.2:g.157078048del GRCh38
NC_000004.11:g.157999200del , CM000666.1:g.157999200del GRCh37
NC_000004.10:g.158218650del NCBI36
NG_015823.1:g.6924del

Transcript Alleles

HGVS Amino-acid Change
NM_000824.5:c.24del MANE Select NP_000815.1:p.Leu10Ter
ENST00000264428.9:c.24del MANE Select ENSP00000264428.4:p.Leu10Ter
NM_000824.4:c.24del NP_000815.1:p.Leu10Ter
NM_001166060.1:c.24del NP_001159532.1:p.Leu10Ter
NM_001166060.2:c.24del NP_001159532.1:p.Leu10Ter
NM_001166061.1:c.24del NP_001159533.1:p.Leu10Ter
NM_001166061.2:c.24del NP_001159533.1:p.Leu10Ter
ENST00000264428.8:c.24del ENSP00000264428.4:p.Leu10Ter
ENST00000506411.5:c.24del ENSP00000422039.1:p.Leu10Ter
ENST00000509282.1:c.24del ENSP00000427186.1:p.Leu10Ter
ENST00000512619.5:c.24del ENSP00000425433.1:p.Leu10Ter
ENST00000515642.5:c.24del ENSP00000421044.1:p.Leu10Ter
ENST00000541722.5:c.24del ENSP00000441873.1:p.Leu10Ter
XM_011531876.1:c.-332del XP_011530178.1:n.-332del
XM_017008035.2:c.24del XP_016863524.1:p.Leu10Ter
XR_001741207.2:n.205del
XR_002959723.1:n.205del