Canonical Allele Identifier: CA1312143
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs761667081

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427902C>A , CM000663.2:g.197427902C>A GRCh38
NC_000001.10:g.197397032C>A , CM000663.1:g.197397032C>A GRCh37
NC_000001.9:g.195663655C>A NCBI36
NG_008483.1:g.164625C>A
NG_008483.2:g.231441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2577C>A MANE Select ENSP00000356370.3:p.Asn859Lys
ENST00000638467.1:c.2577C>A ENSP00000491102.1:p.Asn859Lys
ENST00000681519.1:c.1458C>A ENSP00000505267.1:p.Asn486Lys
ENST00000367397.1:c.720C>A ENSP00000356367.1:p.Asn240Lys
ENST00000367399.6:c.2241C>A ENSP00000356369.2:p.Asn747Lys
ENST00000367400.7:c.2577C>A ENSP00000356370.3:p.Asn859Lys
ENST00000484075.5:c.2577C>A ENSP00000433932.1:p.Asn859Lys
ENST00000535699.5:c.2370C>A ENSP00000438786.1:p.Asn790Lys
ENST00000538660.5:c.2128+5946C>A ENSP00000438091.1:n.2128+5946C>A
NM_001193640.1:c.2241C>A NP_001180569.1:p.Asn747Lys
NM_001257965.1:c.2370C>A NP_001244894.1:p.Asn790Lys
NM_001257966.1:c.2128+5946C>A NP_001244895.1:n.2128+5946C>A
NM_201253.2:c.2577C>A NP_957705.1:p.Asn859Lys
NR_047563.1:n.2578C>A
NR_047564.1:n.2786C>A
XM_011509365.1:c.2577C>A XP_011507667.1:p.Asn859Lys
XM_011509366.1:c.2577C>A XP_011507668.1:p.Asn859Lys
XM_011509367.1:c.2577C>A XP_011507669.1:p.Asn859Lys
XM_011509368.1:c.1995C>A XP_011507670.1:p.Asn665Lys
XM_011509369.1:c.1020C>A XP_011507671.1:p.Asn340Lys
XM_011509365.2:c.2577C>A XP_011507667.1:p.Asn859Lys
XM_011509369.2:c.1020C>A XP_011507671.1:p.Asn340Lys
XM_017000851.1:c.1734C>A XP_016856340.1:p.Asn578Lys
XM_017000852.1:c.2577C>A XP_016856341.1:p.Asn859Lys
NM_201253.3:c.2577C>A MANE Select NP_957705.1:p.Asn859Lys
NM_001193640.2:c.2241C>A NP_001180569.1:p.Asn747Lys
NM_001257965.2:c.2370C>A NP_001244894.1:p.Asn790Lys
NR_047563.2:n.2530C>A
NR_047564.2:n.2738C>A
NM_001257966.2:c.2128+5946C>A NP_001244895.1:n.2128+5946C>A