Canonical Allele Identifier: CA1312363
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435476G>A , CM000663.2:g.197435476G>A GRCh38
NC_000001.10:g.197404606G>A , CM000663.1:g.197404606G>A GRCh37
NC_000001.9:g.195671229G>A NCBI36
NG_008483.1:g.172199G>A
NG_008483.2:g.239015G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.3613G>A MANE Select ENSP00000356370.3:p.Gly1205Arg
ENST00000638467.1:c.3613G>A ENSP00000491102.1:p.Gly1205Arg
ENST00000681519.1:c.2494G>A ENSP00000505267.1:p.Gly832Arg
ENST00000367397.1:c.1756G>A ENSP00000356367.1:p.Gly586Arg
ENST00000367399.6:c.3277G>A ENSP00000356369.2:p.Gly1093Arg
ENST00000367400.7:c.3613G>A ENSP00000356370.3:p.Gly1205Arg
ENST00000484075.5:c.3613G>A ENSP00000433932.1:p.Gly1205Arg
ENST00000535699.5:c.3541G>A ENSP00000438786.1:p.Gly1181Arg
ENST00000538660.5:c.2129-124G>A ENSP00000438091.1:n.2129-124G>A
NM_001193640.1:c.3277G>A NP_001180569.1:p.Gly1093Arg
NM_001257965.1:c.3541G>A NP_001244894.1:p.Gly1181Arg
NM_001257966.1:c.2129-124G>A NP_001244895.1:n.2129-124G>A
NM_201253.2:c.3613G>A NP_957705.1:p.Gly1205Arg
NR_047563.1:n.3614G>A
NR_047564.1:n.3822G>A
XM_011509365.1:c.3613G>A XP_011507667.1:p.Gly1205Arg
XM_011509366.1:c.3613G>A XP_011507668.1:p.Gly1205Arg
XM_011509367.1:c.3613G>A XP_011507669.1:p.Gly1205Arg
XM_011509368.1:c.3031G>A XP_011507670.1:p.Gly1011Arg
XM_011509369.1:c.2056G>A XP_011507671.1:p.Gly686Arg
XM_011509365.2:c.3613G>A XP_011507667.1:p.Gly1205Arg
XM_011509369.2:c.2056G>A XP_011507671.1:p.Gly686Arg
XM_017000851.1:c.2770G>A XP_016856340.1:p.Gly924Arg
XM_017000852.1:c.3748G>A XP_016856341.1:p.Gly1250Arg
NM_201253.3:c.3613G>A MANE Select NP_957705.1:p.Gly1205Arg
NM_001193640.2:c.3277G>A NP_001180569.1:p.Gly1093Arg
NM_001257965.2:c.3541G>A NP_001244894.1:p.Gly1181Arg
NR_047563.2:n.3566G>A
NR_047564.2:n.3774G>A
NM_001257966.2:c.2129-124G>A NP_001244895.1:n.2129-124G>A