Canonical Allele Identifier: CA344035532
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197477730A>C , CM000663.2:g.197477730A>C GRCh38
NC_000001.10:g.197446860A>C , CM000663.1:g.197446860A>C GRCh37
NC_000001.9:g.195713483A>C NCBI36
NG_008483.1:g.214453A>C
NG_008483.2:g.281269A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.4072A>C MANE Select ENSP00000356370.3:p.Ile1358Leu
ENST00000367399.6:c.3736A>C ENSP00000356369.2:p.Ile1246Leu
ENST00000367400.7:c.4072A>C ENSP00000356370.3:p.Ile1358Leu
ENST00000448952.1:c.306A>C ENSP00000395407.1:n.306A>C
ENST00000484075.5:c.*183A>C ENSP00000433932.1:n.*183A>C
ENST00000535699.5:c.4000A>C ENSP00000438786.1:p.Ile1334Leu
ENST00000538660.5:c.2464A>C ENSP00000438091.1:p.Ile822Leu
NM_001193640.1:c.3736A>C NP_001180569.1:p.Ile1246Leu
NM_001257965.1:c.4000A>C NP_001244894.1:p.Ile1334Leu
NM_001257966.1:c.2464A>C NP_001244895.1:p.Ile822Leu
NM_201253.2:c.4072A>C NP_957705.1:p.Ile1358Leu
NR_047563.1:n.4073A>C
NR_047564.1:n.4523A>C
XM_011509366.1:c.*177A>C XP_011507668.1:n.*177A>C
XM_011509367.1:c.*51A>C XP_011507669.1:n.*51A>C
XM_011509368.1:c.3490A>C XP_011507670.1:p.Ile1164Leu
XM_011509369.1:c.2515A>C XP_011507671.1:p.Ile839Leu
XM_011509369.2:c.2515A>C XP_011507671.1:p.Ile839Leu
XM_017000851.1:c.3229A>C XP_016856340.1:p.Ile1077Leu
XM_017000852.1:c.4207A>C XP_016856341.1:p.Ile1403Leu
NM_201253.3:c.4072A>C MANE Select NP_957705.1:p.Ile1358Leu
NM_001193640.2:c.3736A>C NP_001180569.1:p.Ile1246Leu
NM_001257965.2:c.4000A>C NP_001244894.1:p.Ile1334Leu
NR_047563.2:n.4025A>C
NR_047564.2:n.4475A>C
NM_001257966.2:c.2464A>C NP_001244895.1:p.Ile822Leu