Canonical Allele Identifier: CA344037307
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427754C>A , CM000663.2:g.197427754C>A GRCh38
NC_000001.10:g.197396884C>A , CM000663.1:g.197396884C>A GRCh37
NC_000001.9:g.195663507C>A NCBI36
NG_008483.1:g.164477C>A
NG_008483.2:g.231293C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2429C>A MANE Select ENSP00000356370.3:p.Ser810Tyr
ENST00000638467.1:c.2429C>A ENSP00000491102.1:p.Ser810Tyr
ENST00000681519.1:c.1310C>A ENSP00000505267.1:p.Ser437Tyr
ENST00000367397.1:c.572C>A ENSP00000356367.1:p.Ser191Tyr
ENST00000367399.6:c.2093C>A ENSP00000356369.2:p.Ser698Tyr
ENST00000367400.7:c.2429C>A ENSP00000356370.3:p.Ser810Tyr
ENST00000480086.2:n.330C>A
ENST00000484075.5:c.2429C>A ENSP00000433932.1:p.Ser810Tyr
ENST00000535699.5:c.2222C>A ENSP00000438786.1:p.Ser741Tyr
ENST00000538660.5:c.2128+5798C>A ENSP00000438091.1:n.2128+5798C>A
NM_001193640.1:c.2093C>A NP_001180569.1:p.Ser698Tyr
NM_001257965.1:c.2222C>A NP_001244894.1:p.Ser741Tyr
NM_001257966.1:c.2128+5798C>A NP_001244895.1:n.2128+5798C>A
NM_201253.2:c.2429C>A NP_957705.1:p.Ser810Tyr
NR_047563.1:n.2430C>A
NR_047564.1:n.2638C>A
XM_011509365.1:c.2429C>A XP_011507667.1:p.Ser810Tyr
XM_011509366.1:c.2429C>A XP_011507668.1:p.Ser810Tyr
XM_011509367.1:c.2429C>A XP_011507669.1:p.Ser810Tyr
XM_011509368.1:c.1847C>A XP_011507670.1:p.Ser616Tyr
XM_011509369.1:c.872C>A XP_011507671.1:p.Ser291Tyr
XM_011509365.2:c.2429C>A XP_011507667.1:p.Ser810Tyr
XM_011509369.2:c.872C>A XP_011507671.1:p.Ser291Tyr
XM_017000851.1:c.1586C>A XP_016856340.1:p.Ser529Tyr
XM_017000852.1:c.2429C>A XP_016856341.1:p.Ser810Tyr
NM_201253.3:c.2429C>A MANE Select NP_957705.1:p.Ser810Tyr
NM_001193640.2:c.2093C>A NP_001180569.1:p.Ser698Tyr
NM_001257965.2:c.2222C>A NP_001244894.1:p.Ser741Tyr
NR_047563.2:n.2382C>A
NR_047564.2:n.2590C>A
NM_001257966.2:c.2128+5798C>A NP_001244895.1:n.2128+5798C>A