Canonical Allele Identifier: CA344033053
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421779A>T , CM000663.2:g.197421779A>T GRCh38
NC_000001.10:g.197390909A>T , CM000663.1:g.197390909A>T GRCh37
NC_000001.9:g.195657532A>T NCBI36
NG_008483.1:g.158502A>T
NG_008483.2:g.225318A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1951A>T MANE Select ENSP00000356370.3:p.Asn651Tyr
ENST00000638467.1:c.1951A>T ENSP00000491102.1:p.Asn651Tyr
ENST00000681519.1:c.832A>T ENSP00000505267.1:p.Asn278Tyr
ENST00000367397.1:c.94A>T ENSP00000356367.1:p.Asn32Tyr
ENST00000367399.6:c.1615A>T ENSP00000356369.2:p.Asn539Tyr
ENST00000367400.7:c.1951A>T ENSP00000356370.3:p.Asn651Tyr
ENST00000484075.5:c.1951A>T ENSP00000433932.1:p.Asn651Tyr
ENST00000535699.5:c.1744A>T ENSP00000438786.1:p.Asn582Tyr
ENST00000538660.5:c.1951A>T ENSP00000438091.1:p.Asn651Tyr
NM_001193640.1:c.1615A>T NP_001180569.1:p.Asn539Tyr
NM_001257965.1:c.1744A>T NP_001244894.1:p.Asn582Tyr
NM_001257966.1:c.1951A>T NP_001244895.1:p.Asn651Tyr
NM_201253.2:c.1951A>T NP_957705.1:p.Asn651Tyr
NR_047563.1:n.1952A>T
NR_047564.1:n.2160A>T
XM_011509365.1:c.1951A>T XP_011507667.1:p.Asn651Tyr
XM_011509366.1:c.1951A>T XP_011507668.1:p.Asn651Tyr
XM_011509367.1:c.1951A>T XP_011507669.1:p.Asn651Tyr
XM_011509368.1:c.1369A>T XP_011507670.1:p.Asn457Tyr
XM_011509369.1:c.394A>T XP_011507671.1:p.Asn132Tyr
XM_011509365.2:c.1951A>T XP_011507667.1:p.Asn651Tyr
XM_011509369.2:c.394A>T XP_011507671.1:p.Asn132Tyr
XM_017000851.1:c.1108A>T XP_016856340.1:p.Asn370Tyr
XM_017000852.1:c.1951A>T XP_016856341.1:p.Asn651Tyr
NM_201253.3:c.1951A>T MANE Select NP_957705.1:p.Asn651Tyr
NM_001193640.2:c.1615A>T NP_001180569.1:p.Asn539Tyr
NM_001257965.2:c.1744A>T NP_001244894.1:p.Asn582Tyr
NR_047563.2:n.1904A>T
NR_047564.2:n.2112A>T
NM_001257966.2:c.1951A>T NP_001244895.1:p.Asn651Tyr