Canonical Allele Identifier: CA1506148478
Gene: GLRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136750_157136751delinsAT , CM000666.2:g.157136750_157136751delinsAT GRCh38
NC_000004.11:g.158057902_158057903delinsAT , CM000666.1:g.158057902_158057903delinsAT GRCh37
NC_000004.10:g.158277352_158277353delinsAT NCBI36
NG_015823.1:g.65626_65627delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.527+52_528-53delinsAT MANE Select ENSP00000264428.4:n.527+52_528-53delinsAT
ENST00000264428.8:c.527+52_528-53delinsAT ENSP00000264428.4:n.527+52_528-53delinsAT
ENST00000506411.5:c.*447+52_*448-53delinsAT ENSP00000422039.1:n.*447+52_*448-53delinsAT
ENST00000509282.1:c.527+52_528-53delinsAT ENSP00000427186.1:n.527+52_528-53delinsAT
ENST00000510970.1:n.334+52_335-53delinsAT
ENST00000512619.5:c.123-33682_123-33681delinsAT ENSP00000425433.1:n.123-33682_123-33681delinsAT
ENST00000541722.5:c.527+52_528-53delinsAT ENSP00000441873.1:n.527+52_528-53delinsAT
NM_000824.4:c.527+52_528-53delinsAT NP_000815.1:n.527+52_528-53delinsAT
NM_001166060.1:c.527+52_528-53delinsAT NP_001159532.1:n.527+52_528-53delinsAT
NM_001166061.1:c.527+52_528-53delinsAT NP_001159533.1:n.527+52_528-53delinsAT
XM_011531876.1:c.233+52_234-53delinsAT XP_011530178.1:n.233+52_234-53delinsAT
XM_017008034.1:c.233+52_234-53delinsAT XP_016863523.1:n.233+52_234-53delinsAT
XM_017008035.2:c.527+52_528-53delinsAT XP_016863524.1:n.527+52_528-53delinsAT
XR_001741207.2:n.708+52_709-53delinsAT
XR_002959723.1:n.708+52_709-53delinsAT
NM_000824.5:c.527+52_528-53delinsAT MANE Select NP_000815.1:n.527+52_528-53delinsAT
NM_001166060.2:c.527+52_528-53delinsAT NP_001159532.1:n.527+52_528-53delinsAT
NM_001166061.2:c.527+52_528-53delinsAT NP_001159533.1:n.527+52_528-53delinsAT