Canonical Allele Identifier: CA344033050
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1951A>G MANE Select ENSP00000356370.3:p.Asn651Asp
ENST00000638467.1:c.1951A>G ENSP00000491102.1:p.Asn651Asp
ENST00000681519.1:c.832A>G ENSP00000505267.1:p.Asn278Asp
ENST00000367397.1:c.94A>G ENSP00000356367.1:p.Asn32Asp
ENST00000367399.6:c.1615A>G ENSP00000356369.2:p.Asn539Asp
ENST00000367400.7:c.1951A>G ENSP00000356370.3:p.Asn651Asp
ENST00000484075.5:c.1951A>G ENSP00000433932.1:p.Asn651Asp
ENST00000535699.5:c.1744A>G ENSP00000438786.1:p.Asn582Asp
ENST00000538660.5:c.1951A>G ENSP00000438091.1:p.Asn651Asp
NM_001193640.1:c.1615A>G NP_001180569.1:p.Asn539Asp
NM_001257965.1:c.1744A>G NP_001244894.1:p.Asn582Asp
NM_001257966.1:c.1951A>G NP_001244895.1:p.Asn651Asp
NM_201253.2:c.1951A>G NP_957705.1:p.Asn651Asp
NR_047563.1:n.1952A>G
NR_047564.1:n.2160A>G
XM_011509365.1:c.1951A>G XP_011507667.1:p.Asn651Asp
XM_011509366.1:c.1951A>G XP_011507668.1:p.Asn651Asp
XM_011509367.1:c.1951A>G XP_011507669.1:p.Asn651Asp
XM_011509368.1:c.1369A>G XP_011507670.1:p.Asn457Asp
XM_011509369.1:c.394A>G XP_011507671.1:p.Asn132Asp
XM_011509365.2:c.1951A>G XP_011507667.1:p.Asn651Asp
XM_011509369.2:c.394A>G XP_011507671.1:p.Asn132Asp
XM_017000851.1:c.1108A>G XP_016856340.1:p.Asn370Asp
XM_017000852.1:c.1951A>G XP_016856341.1:p.Asn651Asp
NM_201253.3:c.1951A>G MANE Select NP_957705.1:p.Asn651Asp
NM_001193640.2:c.1615A>G NP_001180569.1:p.Asn539Asp
NM_001257965.2:c.1744A>G NP_001244894.1:p.Asn582Asp
NR_047563.2:n.1904A>G
NR_047564.2:n.2112A>G
NM_001257966.2:c.1951A>G NP_001244895.1:p.Asn651Asp