Canonical Allele Identifier: CA344033201
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421806T>A , CM000663.2:g.197421806T>A GRCh38
NC_000001.10:g.197390936T>A , CM000663.1:g.197390936T>A GRCh37
NC_000001.9:g.195657559T>A NCBI36
NG_008483.1:g.158529T>A
NG_008483.2:g.225345T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1978T>A MANE Select ENSP00000356370.3:p.Ser660Thr
ENST00000638467.1:c.1978T>A ENSP00000491102.1:p.Ser660Thr
ENST00000681519.1:c.859T>A ENSP00000505267.1:p.Ser287Thr
ENST00000367397.1:c.121T>A ENSP00000356367.1:p.Ser41Thr
ENST00000367399.6:c.1642T>A ENSP00000356369.2:p.Ser548Thr
ENST00000367400.7:c.1978T>A ENSP00000356370.3:p.Ser660Thr
ENST00000484075.5:c.1978T>A ENSP00000433932.1:p.Ser660Thr
ENST00000535699.5:c.1771T>A ENSP00000438786.1:p.Ser591Thr
ENST00000538660.5:c.1978T>A ENSP00000438091.1:p.Ser660Thr
NM_001193640.1:c.1642T>A NP_001180569.1:p.Ser548Thr
NM_001257965.1:c.1771T>A NP_001244894.1:p.Ser591Thr
NM_001257966.1:c.1978T>A NP_001244895.1:p.Ser660Thr
NM_201253.2:c.1978T>A NP_957705.1:p.Ser660Thr
NR_047563.1:n.1979T>A
NR_047564.1:n.2187T>A
XM_011509365.1:c.1978T>A XP_011507667.1:p.Ser660Thr
XM_011509366.1:c.1978T>A XP_011507668.1:p.Ser660Thr
XM_011509367.1:c.1978T>A XP_011507669.1:p.Ser660Thr
XM_011509368.1:c.1396T>A XP_011507670.1:p.Ser466Thr
XM_011509369.1:c.421T>A XP_011507671.1:p.Ser141Thr
XM_011509365.2:c.1978T>A XP_011507667.1:p.Ser660Thr
XM_011509369.2:c.421T>A XP_011507671.1:p.Ser141Thr
XM_017000851.1:c.1135T>A XP_016856340.1:p.Ser379Thr
XM_017000852.1:c.1978T>A XP_016856341.1:p.Ser660Thr
NM_201253.3:c.1978T>A MANE Select NP_957705.1:p.Ser660Thr
NM_001193640.2:c.1642T>A NP_001180569.1:p.Ser548Thr
NM_001257965.2:c.1771T>A NP_001244894.1:p.Ser591Thr
NR_047563.2:n.1931T>A
NR_047564.2:n.2139T>A
NM_001257966.2:c.1978T>A NP_001244895.1:p.Ser660Thr