Canonical Allele Identifier: CA344030713
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421224G>A , CM000663.2:g.197421224G>A GRCh38
NC_000001.10:g.197390354G>A , CM000663.1:g.197390354G>A GRCh37
NC_000001.9:g.195656977G>A NCBI36
NG_008483.1:g.157947G>A
NG_008483.2:g.224763G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1396G>A MANE Select ENSP00000356370.3:p.Gly466Arg
ENST00000638467.1:c.1396G>A ENSP00000491102.1:p.Gly466Arg
ENST00000681519.1:c.277G>A ENSP00000505267.1:p.Gly93Arg
ENST00000367397.1:c.-462G>A ENSP00000356367.1:n.-462G>A
ENST00000367399.6:c.1060G>A ENSP00000356369.2:p.Gly354Arg
ENST00000367400.7:c.1396G>A ENSP00000356370.3:p.Gly466Arg
ENST00000476483.1:n.356G>A
ENST00000484075.5:c.1396G>A ENSP00000433932.1:p.Gly466Arg
ENST00000535699.5:c.1189G>A ENSP00000438786.1:p.Gly397Arg
ENST00000538660.5:c.1396G>A ENSP00000438091.1:p.Gly466Arg
NM_001193640.1:c.1060G>A NP_001180569.1:p.Gly354Arg
NM_001257965.1:c.1189G>A NP_001244894.1:p.Gly397Arg
NM_001257966.1:c.1396G>A NP_001244895.1:p.Gly466Arg
NM_201253.2:c.1396G>A NP_957705.1:p.Gly466Arg
NR_047563.1:n.1605G>A
NR_047564.1:n.1605G>A
XM_011509365.1:c.1396G>A XP_011507667.1:p.Gly466Arg
XM_011509366.1:c.1396G>A XP_011507668.1:p.Gly466Arg
XM_011509367.1:c.1396G>A XP_011507669.1:p.Gly466Arg
XM_011509368.1:c.814G>A XP_011507670.1:p.Gly272Arg
XM_011509369.1:c.-162G>A XP_011507671.1:n.-162G>A
XM_011509365.2:c.1396G>A XP_011507667.1:p.Gly466Arg
XM_011509369.2:c.-162G>A XP_011507671.1:n.-162G>A
XM_017000851.1:c.553G>A XP_016856340.1:p.Gly185Arg
XM_017000852.1:c.1396G>A XP_016856341.1:p.Gly466Arg
NM_201253.3:c.1396G>A MANE Select NP_957705.1:p.Gly466Arg
NM_001193640.2:c.1060G>A NP_001180569.1:p.Gly354Arg
NM_001257965.2:c.1189G>A NP_001244894.1:p.Gly397Arg
NR_047563.2:n.1557G>A
NR_047564.2:n.1557G>A
NM_001257966.2:c.1396G>A NP_001244895.1:p.Gly466Arg