Canonical Allele Identifier: CA344030541
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421187T>G , CM000663.2:g.197421187T>G GRCh38
NC_000001.10:g.197390317T>G , CM000663.1:g.197390317T>G GRCh37
NC_000001.9:g.195656940T>G NCBI36
NG_008483.1:g.157910T>G
NG_008483.2:g.224726T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1359T>G MANE Select ENSP00000356370.3:p.Asn453Lys
ENST00000638467.1:c.1359T>G ENSP00000491102.1:p.Asn453Lys
ENST00000681519.1:c.240T>G ENSP00000505267.1:p.Asn80Lys
ENST00000367397.1:c.-499T>G ENSP00000356367.1:n.-499T>G
ENST00000367399.6:c.1023T>G ENSP00000356369.2:p.Asn341Lys
ENST00000367400.7:c.1359T>G ENSP00000356370.3:p.Asn453Lys
ENST00000476483.1:n.319T>G
ENST00000484075.5:c.1359T>G ENSP00000433932.1:p.Asn453Lys
ENST00000535699.5:c.1152T>G ENSP00000438786.1:p.Asn384Lys
ENST00000538660.5:c.1359T>G ENSP00000438091.1:p.Asn453Lys
NM_001193640.1:c.1023T>G NP_001180569.1:p.Asn341Lys
NM_001257965.1:c.1152T>G NP_001244894.1:p.Asn384Lys
NM_001257966.1:c.1359T>G NP_001244895.1:p.Asn453Lys
NM_201253.2:c.1359T>G NP_957705.1:p.Asn453Lys
NR_047563.1:n.1568T>G
NR_047564.1:n.1568T>G
XM_011509365.1:c.1359T>G XP_011507667.1:p.Asn453Lys
XM_011509366.1:c.1359T>G XP_011507668.1:p.Asn453Lys
XM_011509367.1:c.1359T>G XP_011507669.1:p.Asn453Lys
XM_011509368.1:c.777T>G XP_011507670.1:p.Asn259Lys
XM_011509369.1:c.-199T>G XP_011507671.1:n.-199T>G
XM_011509365.2:c.1359T>G XP_011507667.1:p.Asn453Lys
XM_011509369.2:c.-199T>G XP_011507671.1:n.-199T>G
XM_017000851.1:c.516T>G XP_016856340.1:p.Asn172Lys
XM_017000852.1:c.1359T>G XP_016856341.1:p.Asn453Lys
NM_201253.3:c.1359T>G MANE Select NP_957705.1:p.Asn453Lys
NM_001193640.2:c.1023T>G NP_001180569.1:p.Asn341Lys
NM_001257965.2:c.1152T>G NP_001244894.1:p.Asn384Lys
NR_047563.2:n.1520T>G
NR_047564.2:n.1520T>G
NM_001257966.2:c.1359T>G NP_001244895.1:p.Asn453Lys