Canonical Allele Identifier: CA344051056
Community Standard Title: NM_201253.3(CRB1):c.3878G>A (p.Trp1293Ter)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197438675G>A , CM000663.2:g.197438675G>A GRCh38
NC_000001.10:g.197407805G>A , CM000663.1:g.197407805G>A GRCh37
NC_000001.9:g.195674428G>A NCBI36
NG_008483.1:g.175398G>A
NG_008483.2:g.242214G>A

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.3878G>A MANE Select NP_957705.1:p.Trp1293Ter
ENST00000367400.8:c.3878G>A MANE Select ENSP00000356370.3:p.Trp1293Ter
NM_001193640.1:c.3542G>A NP_001180569.1:p.Trp1181Ter
NM_001193640.2:c.3542G>A NP_001180569.1:p.Trp1181Ter
NM_001257965.1:c.3806G>A NP_001244894.1:p.Trp1269Ter
NM_001257965.2:c.3806G>A NP_001244894.1:p.Trp1269Ter
NM_001257966.1:c.2270G>A NP_001244895.1:p.Trp757Ter
NM_001257966.2:c.2270G>A NP_001244895.1:p.Trp757Ter
NM_201253.2:c.3878G>A NP_957705.1:p.Trp1293Ter
NR_047563.1:n.3879G>A
NR_047563.2:n.3831G>A
NR_047564.1:n.4087G>A
NR_047564.2:n.4039G>A
ENST00000367397.1:c.2021G>A ENSP00000356367.1:p.Trp674Ter
ENST00000367399.6:c.3542G>A ENSP00000356369.2:p.Trp1181Ter
ENST00000367400.7:c.3878G>A ENSP00000356370.3:p.Trp1293Ter
ENST00000484075.5:c.3878G>A ENSP00000433932.1:p.Trp1293Ter
ENST00000535699.5:c.3806G>A ENSP00000438786.1:p.Trp1269Ter
ENST00000538660.5:c.2270G>A ENSP00000438091.1:p.Trp757Ter
ENST00000638467.1:c.3878G>A ENSP00000491102.1:p.Trp1293Ter
ENST00000681519.1:c.2759G>A ENSP00000505267.1:p.Trp920Ter
XM_011509365.1:c.3878G>A XP_011507667.1:p.Trp1293Ter
XM_011509365.2:c.3878G>A XP_011507667.1:p.Trp1293Ter
XM_011509366.1:c.3878G>A XP_011507668.1:p.Trp1293Ter
XM_011509367.1:c.3878G>A XP_011507669.1:p.Cys1293Tyr
XM_011509368.1:c.3296G>A XP_011507670.1:p.Trp1099Ter
XM_011509369.1:c.2321G>A XP_011507671.1:p.Trp774Ter
XM_011509369.2:c.2321G>A XP_011507671.1:p.Trp774Ter
XM_017000851.1:c.3035G>A XP_016856340.1:p.Trp1012Ter
XM_017000852.1:c.4013G>A XP_016856341.1:p.Trp1338Ter