Canonical Allele Identifier: CA344032891
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421741C>G , CM000663.2:g.197421741C>G GRCh38
NC_000001.10:g.197390871C>G , CM000663.1:g.197390871C>G GRCh37
NC_000001.9:g.195657494C>G NCBI36
NG_008483.1:g.158464C>G
NG_008483.2:g.225280C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1913C>G MANE Select ENSP00000356370.3:p.Ser638Trp
ENST00000638467.1:c.1913C>G ENSP00000491102.1:p.Ser638Trp
ENST00000681519.1:c.794C>G ENSP00000505267.1:p.Ser265Trp
ENST00000367397.1:c.56C>G ENSP00000356367.1:p.Ser19Trp
ENST00000367399.6:c.1577C>G ENSP00000356369.2:p.Ser526Trp
ENST00000367400.7:c.1913C>G ENSP00000356370.3:p.Ser638Trp
ENST00000484075.5:c.1913C>G ENSP00000433932.1:p.Ser638Trp
ENST00000535699.5:c.1706C>G ENSP00000438786.1:p.Ser569Trp
ENST00000538660.5:c.1913C>G ENSP00000438091.1:p.Ser638Trp
NM_001193640.1:c.1577C>G NP_001180569.1:p.Ser526Trp
NM_001257965.1:c.1706C>G NP_001244894.1:p.Ser569Trp
NM_001257966.1:c.1913C>G NP_001244895.1:p.Ser638Trp
NM_201253.2:c.1913C>G NP_957705.1:p.Ser638Trp
NR_047563.1:n.1923-9C>G
NR_047564.1:n.2122C>G
XM_011509365.1:c.1913C>G XP_011507667.1:p.Ser638Trp
XM_011509366.1:c.1913C>G XP_011507668.1:p.Ser638Trp
XM_011509367.1:c.1913C>G XP_011507669.1:p.Ser638Trp
XM_011509368.1:c.1331C>G XP_011507670.1:p.Ser444Trp
XM_011509369.1:c.356C>G XP_011507671.1:p.Ser119Trp
XM_011509365.2:c.1913C>G XP_011507667.1:p.Ser638Trp
XM_011509369.2:c.356C>G XP_011507671.1:p.Ser119Trp
XM_017000851.1:c.1070C>G XP_016856340.1:p.Ser357Trp
XM_017000852.1:c.1913C>G XP_016856341.1:p.Ser638Trp
NM_201253.3:c.1913C>G MANE Select NP_957705.1:p.Ser638Trp
NM_001193640.2:c.1577C>G NP_001180569.1:p.Ser526Trp
NM_001257965.2:c.1706C>G NP_001244894.1:p.Ser569Trp
NR_047563.2:n.1875-9C>G
NR_047564.2:n.2074C>G
NM_001257966.2:c.1913C>G NP_001244895.1:p.Ser638Trp