Canonical Allele Identifier: CA1218063062
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421261C= , CM000663.2:g.197421261C= GRCh38
NC_000001.10:g.197390391C= , CM000663.1:g.197390391C= GRCh37
NC_000001.9:g.195657014C= NCBI36
NG_008483.1:g.157984C=
NG_008483.2:g.224800C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367400.8:c.1433C= MANE Select ENSP00000356370.3:p.Ser478=
ENST00000638467.1:c.1433C= ENSP00000491102.1:p.Ser478=
ENST00000681519.1:c.314C= ENSP00000505267.1:p.Ser105=
ENST00000367397.1:c.-425C= ENSP00000356367.1:n.-425C=
ENST00000367399.6:c.1097C= ENSP00000356369.2:p.Ser366=
ENST00000367400.7:c.1433C= ENSP00000356370.3:p.Ser478=
ENST00000476483.1:n.393C=
ENST00000484075.5:c.1433C= ENSP00000433932.1:p.Ser478=
ENST00000535699.5:c.1226C= ENSP00000438786.1:p.Ser409=
ENST00000538660.5:c.1433C= ENSP00000438091.1:p.Ser478=
NM_001193640.1:c.1097C= NP_001180569.1:p.Ser366=
NM_001257965.1:c.1226C= NP_001244894.1:p.Ser409=
NM_001257966.1:c.1433C= NP_001244895.1:p.Ser478=
NM_201253.2:c.1433C= NP_957705.1:p.Ser478=
NR_047563.1:n.1642C=
NR_047564.1:n.1642C=
XM_011509365.1:c.1433C= XP_011507667.1:p.Ser478=
XM_011509366.1:c.1433C= XP_011507668.1:p.Ser478=
XM_011509367.1:c.1433C= XP_011507669.1:p.Ser478=
XM_011509368.1:c.851C= XP_011507670.1:p.Ser284=
XM_011509369.1:c.-125C= XP_011507671.1:n.-125C=
XM_011509365.2:c.1433C= XP_011507667.1:p.Ser478=
XM_011509369.2:c.-125C= XP_011507671.1:n.-125C=
XM_017000851.1:c.590C= XP_016856340.1:p.Ser197=
XM_017000852.1:c.1433C= XP_016856341.1:p.Ser478=
NM_201253.3:c.1433C= MANE Select NP_957705.1:p.Ser478=
NM_001193640.2:c.1097C= NP_001180569.1:p.Ser366=
NM_001257965.2:c.1226C= NP_001244894.1:p.Ser409=
NR_047563.2:n.1594C=
NR_047564.2:n.1594C=
NM_001257966.2:c.1433C= NP_001244895.1:p.Ser478=