Canonical Allele Identifier: CA344030269
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421127T>A , CM000663.2:g.197421127T>A GRCh38
NC_000001.10:g.197390257T>A , CM000663.1:g.197390257T>A GRCh37
NC_000001.9:g.195656880T>A NCBI36
NG_008483.1:g.157850T>A
NG_008483.2:g.224666T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1299T>A MANE Select ENSP00000356370.3:p.Tyr433Ter
ENST00000638467.1:c.1299T>A ENSP00000491102.1:p.Tyr433Ter
ENST00000681519.1:c.180T>A ENSP00000505267.1:p.Tyr60Ter
ENST00000367397.1:c.-559T>A ENSP00000356367.1:n.-559T>A
ENST00000367399.6:c.963T>A ENSP00000356369.2:p.Tyr321Ter
ENST00000367400.7:c.1299T>A ENSP00000356370.3:p.Tyr433Ter
ENST00000476483.1:n.259T>A
ENST00000484075.5:c.1299T>A ENSP00000433932.1:p.Tyr433Ter
ENST00000535699.5:c.1092T>A ENSP00000438786.1:p.Tyr364Ter
ENST00000538660.5:c.1299T>A ENSP00000438091.1:p.Tyr433Ter
NM_001193640.1:c.963T>A NP_001180569.1:p.Tyr321Ter
NM_001257965.1:c.1092T>A NP_001244894.1:p.Tyr364Ter
NM_001257966.1:c.1299T>A NP_001244895.1:p.Tyr433Ter
NM_201253.2:c.1299T>A NP_957705.1:p.Tyr433Ter
NR_047563.1:n.1508T>A
NR_047564.1:n.1508T>A
XM_011509365.1:c.1299T>A XP_011507667.1:p.Tyr433Ter
XM_011509366.1:c.1299T>A XP_011507668.1:p.Tyr433Ter
XM_011509367.1:c.1299T>A XP_011507669.1:p.Tyr433Ter
XM_011509368.1:c.717T>A XP_011507670.1:p.Tyr239Ter
XM_011509369.1:c.-259T>A XP_011507671.1:n.-259T>A
XM_011509365.2:c.1299T>A XP_011507667.1:p.Tyr433Ter
XM_011509369.2:c.-259T>A XP_011507671.1:n.-259T>A
XM_017000851.1:c.456T>A XP_016856340.1:p.Tyr152Ter
XM_017000852.1:c.1299T>A XP_016856341.1:p.Tyr433Ter
NM_201253.3:c.1299T>A MANE Select NP_957705.1:p.Tyr433Ter
NM_001193640.2:c.963T>A NP_001180569.1:p.Tyr321Ter
NM_001257965.2:c.1092T>A NP_001244894.1:p.Tyr364Ter
NR_047563.2:n.1460T>A
NR_047564.2:n.1460T>A
NM_001257966.2:c.1299T>A NP_001244895.1:p.Tyr433Ter