Canonical Allele Identifier: CA1147340957
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427728G= , CM000663.2:g.197427728G= GRCh38
NC_000001.10:g.197396858G= , CM000663.1:g.197396858G= GRCh37
NC_000001.9:g.195663481G= NCBI36
NG_008483.1:g.164451G=
NG_008483.2:g.231267G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367400.8:c.2403G= MANE Select ENSP00000356370.3:p.Lys801=
ENST00000638467.1:c.2403G= ENSP00000491102.1:p.Lys801=
ENST00000681519.1:c.1284G= ENSP00000505267.1:p.Lys428=
ENST00000367397.1:c.546G= ENSP00000356367.1:p.Lys182=
ENST00000367399.6:c.2067G= ENSP00000356369.2:p.Lys689=
ENST00000367400.7:c.2403G= ENSP00000356370.3:p.Lys801=
ENST00000480086.2:n.304G=
ENST00000484075.5:c.2403G= ENSP00000433932.1:p.Lys801=
ENST00000535699.5:c.2196G= ENSP00000438786.1:p.Lys732=
ENST00000538660.5:c.2128+5772G= ENSP00000438091.1:n.2128+5772G=
NM_001193640.1:c.2067G= NP_001180569.1:p.Lys689=
NM_001257965.1:c.2196G= NP_001244894.1:p.Lys732=
NM_001257966.1:c.2128+5772G= NP_001244895.1:n.2128+5772G=
NM_201253.2:c.2403G= NP_957705.1:p.Lys801=
NR_047563.1:n.2404G=
NR_047564.1:n.2612G=
XM_011509365.1:c.2403G= XP_011507667.1:p.Lys801=
XM_011509366.1:c.2403G= XP_011507668.1:p.Lys801=
XM_011509367.1:c.2403G= XP_011507669.1:p.Lys801=
XM_011509368.1:c.1821G= XP_011507670.1:p.Lys607=
XM_011509369.1:c.846G= XP_011507671.1:p.Lys282=
XM_011509365.2:c.2403G= XP_011507667.1:p.Lys801=
XM_011509369.2:c.846G= XP_011507671.1:p.Lys282=
XM_017000851.1:c.1560G= XP_016856340.1:p.Lys520=
XM_017000852.1:c.2403G= XP_016856341.1:p.Lys801=
NM_201253.3:c.2403G= MANE Select NP_957705.1:p.Lys801=
NM_001193640.2:c.2067G= NP_001180569.1:p.Lys689=
NM_001257965.2:c.2196G= NP_001244894.1:p.Lys732=
NR_047563.2:n.2356G=
NR_047564.2:n.2564G=
NM_001257966.2:c.2128+5772G= NP_001244895.1:n.2128+5772G=