Canonical Allele Identifier: CA344035462
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197477693C>A , CM000663.2:g.197477693C>A GRCh38
NC_000001.10:g.197446823C>A , CM000663.1:g.197446823C>A GRCh37
NC_000001.9:g.195713446C>A NCBI36
NG_008483.1:g.214416C>A
NG_008483.2:g.281232C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.4035C>A MANE Select ENSP00000356370.3:p.Phe1345Leu
ENST00000367399.6:c.3699C>A ENSP00000356369.2:p.Phe1233Leu
ENST00000367400.7:c.4035C>A ENSP00000356370.3:p.Phe1345Leu
ENST00000448952.1:c.269C>A ENSP00000395407.1:n.269C>A
ENST00000484075.5:c.*146C>A ENSP00000433932.1:n.*146C>A
ENST00000535699.5:c.3963C>A ENSP00000438786.1:p.Phe1321Leu
ENST00000538660.5:c.2427C>A ENSP00000438091.1:p.Phe809Leu
NM_001193640.1:c.3699C>A NP_001180569.1:p.Phe1233Leu
NM_001257965.1:c.3963C>A NP_001244894.1:p.Phe1321Leu
NM_001257966.1:c.2427C>A NP_001244895.1:p.Phe809Leu
NM_201253.2:c.4035C>A NP_957705.1:p.Phe1345Leu
NR_047563.1:n.4036C>A
NR_047564.1:n.4486C>A
XM_011509366.1:c.*140C>A XP_011507668.1:n.*140C>A
XM_011509367.1:c.*14C>A XP_011507669.1:n.*14C>A
XM_011509368.1:c.3453C>A XP_011507670.1:p.Phe1151Leu
XM_011509369.1:c.2478C>A XP_011507671.1:p.Phe826Leu
XM_011509369.2:c.2478C>A XP_011507671.1:p.Phe826Leu
XM_017000851.1:c.3192C>A XP_016856340.1:p.Phe1064Leu
XM_017000852.1:c.4170C>A XP_016856341.1:p.Phe1390Leu
NM_201253.3:c.4035C>A MANE Select NP_957705.1:p.Phe1345Leu
NM_001193640.2:c.3699C>A NP_001180569.1:p.Phe1233Leu
NM_001257965.2:c.3963C>A NP_001244894.1:p.Phe1321Leu
NR_047563.2:n.3988C>A
NR_047564.2:n.4438C>A
NM_001257966.2:c.2427C>A NP_001244895.1:p.Phe809Leu