Canonical Allele Identifier: CA344032792
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421696A>C , CM000663.2:g.197421696A>C GRCh38
NC_000001.10:g.197390826A>C , CM000663.1:g.197390826A>C GRCh37
NC_000001.9:g.195657449A>C NCBI36
NG_008483.1:g.158419A>C
NG_008483.2:g.225235A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1868A>C MANE Select ENSP00000356370.3:p.Asn623Thr
ENST00000638467.1:c.1868A>C ENSP00000491102.1:p.Asn623Thr
ENST00000681519.1:c.749A>C ENSP00000505267.1:p.Asn250Thr
ENST00000367397.1:c.11A>C ENSP00000356367.1:p.Asn4Thr
ENST00000367399.6:c.1532A>C ENSP00000356369.2:p.Asn511Thr
ENST00000367400.7:c.1868A>C ENSP00000356370.3:p.Asn623Thr
ENST00000484075.5:c.1868A>C ENSP00000433932.1:p.Asn623Thr
ENST00000535699.5:c.1661A>C ENSP00000438786.1:p.Asn554Thr
ENST00000538660.5:c.1868A>C ENSP00000438091.1:p.Asn623Thr
NM_001193640.1:c.1532A>C NP_001180569.1:p.Asn511Thr
NM_001257965.1:c.1661A>C NP_001244894.1:p.Asn554Thr
NM_001257966.1:c.1868A>C NP_001244895.1:p.Asn623Thr
NM_201253.2:c.1868A>C NP_957705.1:p.Asn623Thr
NR_047563.1:n.1923-54A>C
NR_047564.1:n.2077A>C
XM_011509365.1:c.1868A>C XP_011507667.1:p.Asn623Thr
XM_011509366.1:c.1868A>C XP_011507668.1:p.Asn623Thr
XM_011509367.1:c.1868A>C XP_011507669.1:p.Asn623Thr
XM_011509368.1:c.1286A>C XP_011507670.1:p.Asn429Thr
XM_011509369.1:c.311A>C XP_011507671.1:p.Asn104Thr
XM_011509365.2:c.1868A>C XP_011507667.1:p.Asn623Thr
XM_011509369.2:c.311A>C XP_011507671.1:p.Asn104Thr
XM_017000851.1:c.1025A>C XP_016856340.1:p.Asn342Thr
XM_017000852.1:c.1868A>C XP_016856341.1:p.Asn623Thr
NM_201253.3:c.1868A>C MANE Select NP_957705.1:p.Asn623Thr
NM_001193640.2:c.1532A>C NP_001180569.1:p.Asn511Thr
NM_001257965.2:c.1661A>C NP_001244894.1:p.Asn554Thr
NR_047563.2:n.1875-54A>C
NR_047564.2:n.2029A>C
NM_001257966.2:c.1868A>C NP_001244895.1:p.Asn623Thr