Canonical Allele Identifier: CA344047023
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1665083389

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435164G>A , CM000663.2:g.197435164G>A GRCh38
NC_000001.10:g.197404294G>A , CM000663.1:g.197404294G>A GRCh37
NC_000001.9:g.195670917G>A NCBI36
NG_008483.1:g.171887G>A
NG_008483.2:g.238703G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.3301G>A MANE Select ENSP00000356370.3:p.Glu1101Lys
ENST00000638467.1:c.3301G>A ENSP00000491102.1:p.Glu1101Lys
ENST00000681519.1:c.2182G>A ENSP00000505267.1:p.Glu728Lys
ENST00000367397.1:c.1444G>A ENSP00000356367.1:p.Glu482Lys
ENST00000367399.6:c.2965G>A ENSP00000356369.2:p.Glu989Lys
ENST00000367400.7:c.3301G>A ENSP00000356370.3:p.Glu1101Lys
ENST00000484075.5:c.3301G>A ENSP00000433932.1:p.Glu1101Lys
ENST00000535699.5:c.3229G>A ENSP00000438786.1:p.Glu1077Lys
ENST00000538660.5:c.2129-436G>A ENSP00000438091.1:n.2129-436G>A
NM_001193640.1:c.2965G>A NP_001180569.1:p.Glu989Lys
NM_001257965.1:c.3229G>A NP_001244894.1:p.Glu1077Lys
NM_001257966.1:c.2129-436G>A NP_001244895.1:n.2129-436G>A
NM_201253.2:c.3301G>A NP_957705.1:p.Glu1101Lys
NR_047563.1:n.3302G>A
NR_047564.1:n.3510G>A
XM_011509365.1:c.3301G>A XP_011507667.1:p.Glu1101Lys
XM_011509366.1:c.3301G>A XP_011507668.1:p.Glu1101Lys
XM_011509367.1:c.3301G>A XP_011507669.1:p.Glu1101Lys
XM_011509368.1:c.2719G>A XP_011507670.1:p.Glu907Lys
XM_011509369.1:c.1744G>A XP_011507671.1:p.Glu582Lys
XM_011509365.2:c.3301G>A XP_011507667.1:p.Glu1101Lys
XM_011509369.2:c.1744G>A XP_011507671.1:p.Glu582Lys
XM_017000851.1:c.2458G>A XP_016856340.1:p.Glu820Lys
XM_017000852.1:c.3436G>A XP_016856341.1:p.Glu1146Lys
NM_201253.3:c.3301G>A MANE Select NP_957705.1:p.Glu1101Lys
NM_001193640.2:c.2965G>A NP_001180569.1:p.Glu989Lys
NM_001257965.2:c.3229G>A NP_001244894.1:p.Glu1077Lys
NR_047563.2:n.3254G>A
NR_047564.2:n.3462G>A
NM_001257966.2:c.2129-436G>A NP_001244895.1:n.2129-436G>A