Canonical Allele Identifier: CA344032642
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421629A>C , CM000663.2:g.197421629A>C GRCh38
NC_000001.10:g.197390759A>C , CM000663.1:g.197390759A>C GRCh37
NC_000001.9:g.195657382A>C NCBI36
NG_008483.1:g.158352A>C
NG_008483.2:g.225168A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1801A>C MANE Select ENSP00000356370.3:p.Ser601Arg
ENST00000638467.1:c.1801A>C ENSP00000491102.1:p.Ser601Arg
ENST00000681519.1:c.682A>C ENSP00000505267.1:p.Ser228Arg
ENST00000367397.1:c.-57A>C ENSP00000356367.1:n.-57A>C
ENST00000367399.6:c.1465A>C ENSP00000356369.2:p.Ser489Arg
ENST00000367400.7:c.1801A>C ENSP00000356370.3:p.Ser601Arg
ENST00000484075.5:c.1801A>C ENSP00000433932.1:p.Ser601Arg
ENST00000535699.5:c.1594A>C ENSP00000438786.1:p.Ser532Arg
ENST00000538660.5:c.1801A>C ENSP00000438091.1:p.Ser601Arg
NM_001193640.1:c.1465A>C NP_001180569.1:p.Ser489Arg
NM_001257965.1:c.1594A>C NP_001244894.1:p.Ser532Arg
NM_001257966.1:c.1801A>C NP_001244895.1:p.Ser601Arg
NM_201253.2:c.1801A>C NP_957705.1:p.Ser601Arg
NR_047563.1:n.1922+88A>C
NR_047564.1:n.2010A>C
XM_011509365.1:c.1801A>C XP_011507667.1:p.Ser601Arg
XM_011509366.1:c.1801A>C XP_011507668.1:p.Ser601Arg
XM_011509367.1:c.1801A>C XP_011507669.1:p.Ser601Arg
XM_011509368.1:c.1219A>C XP_011507670.1:p.Ser407Arg
XM_011509369.1:c.244A>C XP_011507671.1:p.Ser82Arg
XM_011509365.2:c.1801A>C XP_011507667.1:p.Ser601Arg
XM_011509369.2:c.244A>C XP_011507671.1:p.Ser82Arg
XM_017000851.1:c.958A>C XP_016856340.1:p.Ser320Arg
XM_017000852.1:c.1801A>C XP_016856341.1:p.Ser601Arg
NM_201253.3:c.1801A>C MANE Select NP_957705.1:p.Ser601Arg
NM_001193640.2:c.1465A>C NP_001180569.1:p.Ser489Arg
NM_001257965.2:c.1594A>C NP_001244894.1:p.Ser532Arg
NR_047563.2:n.1874+88A>C
NR_047564.2:n.1962A>C
NM_001257966.2:c.1801A>C NP_001244895.1:p.Ser601Arg