Canonical Allele Identifier: CA344037272
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427749T>G , CM000663.2:g.197427749T>G GRCh38
NC_000001.10:g.197396879T>G , CM000663.1:g.197396879T>G GRCh37
NC_000001.9:g.195663502T>G NCBI36
NG_008483.1:g.164472T>G
NG_008483.2:g.231288T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2424T>G MANE Select ENSP00000356370.3:p.Tyr808Ter
ENST00000638467.1:c.2424T>G ENSP00000491102.1:p.Tyr808Ter
ENST00000681519.1:c.1305T>G ENSP00000505267.1:p.Tyr435Ter
ENST00000367397.1:c.567T>G ENSP00000356367.1:p.Tyr189Ter
ENST00000367399.6:c.2088T>G ENSP00000356369.2:p.Tyr696Ter
ENST00000367400.7:c.2424T>G ENSP00000356370.3:p.Tyr808Ter
ENST00000480086.2:n.325T>G
ENST00000484075.5:c.2424T>G ENSP00000433932.1:p.Tyr808Ter
ENST00000535699.5:c.2217T>G ENSP00000438786.1:p.Tyr739Ter
ENST00000538660.5:c.2128+5793T>G ENSP00000438091.1:n.2128+5793T>G
NM_001193640.1:c.2088T>G NP_001180569.1:p.Tyr696Ter
NM_001257965.1:c.2217T>G NP_001244894.1:p.Tyr739Ter
NM_001257966.1:c.2128+5793T>G NP_001244895.1:n.2128+5793T>G
NM_201253.2:c.2424T>G NP_957705.1:p.Tyr808Ter
NR_047563.1:n.2425T>G
NR_047564.1:n.2633T>G
XM_011509365.1:c.2424T>G XP_011507667.1:p.Tyr808Ter
XM_011509366.1:c.2424T>G XP_011507668.1:p.Tyr808Ter
XM_011509367.1:c.2424T>G XP_011507669.1:p.Tyr808Ter
XM_011509368.1:c.1842T>G XP_011507670.1:p.Tyr614Ter
XM_011509369.1:c.867T>G XP_011507671.1:p.Tyr289Ter
XM_011509365.2:c.2424T>G XP_011507667.1:p.Tyr808Ter
XM_011509369.2:c.867T>G XP_011507671.1:p.Tyr289Ter
XM_017000851.1:c.1581T>G XP_016856340.1:p.Tyr527Ter
XM_017000852.1:c.2424T>G XP_016856341.1:p.Tyr808Ter
NM_201253.3:c.2424T>G MANE Select NP_957705.1:p.Tyr808Ter
NM_001193640.2:c.2088T>G NP_001180569.1:p.Tyr696Ter
NM_001257965.2:c.2217T>G NP_001244894.1:p.Tyr739Ter
NR_047563.2:n.2377T>G
NR_047564.2:n.2585T>G
NM_001257966.2:c.2128+5793T>G NP_001244895.1:n.2128+5793T>G