Canonical Allele Identifier: CA1312134
Community Standard Title: NM_201253.3(CRB1):c.2536G>A (p.Gly846Arg)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427861G>A , CM000663.2:g.197427861G>A GRCh38
NC_000001.10:g.197396991G>A , CM000663.1:g.197396991G>A GRCh37
NC_000001.9:g.195663614G>A NCBI36
NG_008483.1:g.164584G>A
NG_008483.2:g.231400G>A

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.2536G>A MANE Select NP_957705.1:p.Gly846Arg
ENST00000367400.8:c.2536G>A MANE Select ENSP00000356370.3:p.Gly846Arg
NM_001193640.1:c.2200G>A NP_001180569.1:p.Gly734Arg
NM_001193640.2:c.2200G>A NP_001180569.1:p.Gly734Arg
NM_001257965.1:c.2329G>A NP_001244894.1:p.Gly777Arg
NM_001257965.2:c.2329G>A NP_001244894.1:p.Gly777Arg
NM_001257966.1:c.2128+5905G>A NP_001244895.1:n.2128+5905G>A
NM_001257966.2:c.2128+5905G>A NP_001244895.1:n.2128+5905G>A
NM_201253.2:c.2536G>A NP_957705.1:p.Gly846Arg
NR_047563.1:n.2537G>A
NR_047563.2:n.2489G>A
NR_047564.1:n.2745G>A
NR_047564.2:n.2697G>A
ENST00000367397.1:c.679G>A ENSP00000356367.1:p.Gly227Arg
ENST00000367399.6:c.2200G>A ENSP00000356369.2:p.Gly734Arg
ENST00000367400.7:c.2536G>A ENSP00000356370.3:p.Gly846Arg
ENST00000484075.5:c.2536G>A ENSP00000433932.1:p.Gly846Arg
ENST00000535699.5:c.2329G>A ENSP00000438786.1:p.Gly777Arg
ENST00000538660.5:c.2128+5905G>A ENSP00000438091.1:n.2128+5905G>A
ENST00000638467.1:c.2536G>A ENSP00000491102.1:p.Gly846Arg
ENST00000681519.1:c.1417G>A ENSP00000505267.1:p.Gly473Arg
XM_011509365.1:c.2536G>A XP_011507667.1:p.Gly846Arg
XM_011509365.2:c.2536G>A XP_011507667.1:p.Gly846Arg
XM_011509366.1:c.2536G>A XP_011507668.1:p.Gly846Arg
XM_011509367.1:c.2536G>A XP_011507669.1:p.Gly846Arg
XM_011509368.1:c.1954G>A XP_011507670.1:p.Gly652Arg
XM_011509369.1:c.979G>A XP_011507671.1:p.Gly327Arg
XM_011509369.2:c.979G>A XP_011507671.1:p.Gly327Arg
XM_017000851.1:c.1693G>A XP_016856340.1:p.Gly565Arg
XM_017000852.1:c.2536G>A XP_016856341.1:p.Gly846Arg