Canonical Allele Identifier: CA1312257
Gene: CRB1 HGNC NCBI

Linked Data

dbSNP Id: rs778596427

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197434847A>G , CM000663.2:g.197434847A>G GRCh38
NC_000001.10:g.197403977A>G , CM000663.1:g.197403977A>G GRCh37
NC_000001.9:g.195670600A>G NCBI36
NG_008483.1:g.171570A>G
NG_008483.2:g.238386A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2984A>G MANE Select ENSP00000356370.3:p.Glu995Gly
ENST00000638467.1:c.2984A>G ENSP00000491102.1:p.Glu995Gly
ENST00000681519.1:c.1865A>G ENSP00000505267.1:p.Glu622Gly
ENST00000367397.1:c.1127A>G ENSP00000356367.1:p.Glu376Gly
ENST00000367399.6:c.2648A>G ENSP00000356369.2:p.Glu883Gly
ENST00000367400.7:c.2984A>G ENSP00000356370.3:p.Glu995Gly
ENST00000484075.5:c.2984A>G ENSP00000433932.1:p.Glu995Gly
ENST00000535699.5:c.2912A>G ENSP00000438786.1:p.Glu971Gly
ENST00000538660.5:c.2129-753A>G ENSP00000438091.1:n.2129-753A>G
NM_001193640.1:c.2648A>G NP_001180569.1:p.Glu883Gly
NM_001257965.1:c.2912A>G NP_001244894.1:p.Glu971Gly
NM_001257966.1:c.2129-753A>G NP_001244895.1:n.2129-753A>G
NM_201253.2:c.2984A>G NP_957705.1:p.Glu995Gly
NR_047563.1:n.2985A>G
NR_047564.1:n.3193A>G
XM_011509365.1:c.2984A>G XP_011507667.1:p.Glu995Gly
XM_011509366.1:c.2984A>G XP_011507668.1:p.Glu995Gly
XM_011509367.1:c.2984A>G XP_011507669.1:p.Glu995Gly
XM_011509368.1:c.2402A>G XP_011507670.1:p.Glu801Gly
XM_011509369.1:c.1427A>G XP_011507671.1:p.Glu476Gly
XM_011509365.2:c.2984A>G XP_011507667.1:p.Glu995Gly
XM_011509369.2:c.1427A>G XP_011507671.1:p.Glu476Gly
XM_017000851.1:c.2141A>G XP_016856340.1:p.Glu714Gly
XM_017000852.1:c.3119A>G XP_016856341.1:p.Glu1040Gly
NM_201253.3:c.2984A>G MANE Select NP_957705.1:p.Glu995Gly
NM_001193640.2:c.2648A>G NP_001180569.1:p.Glu883Gly
NM_001257965.2:c.2912A>G NP_001244894.1:p.Glu971Gly
NR_047563.2:n.2937A>G
NR_047564.2:n.3145A>G
NM_001257966.2:c.2129-753A>G NP_001244895.1:n.2129-753A>G