Canonical Allele Identifier: CA344029936
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421075C>A , CM000663.2:g.197421075C>A GRCh38
NC_000001.10:g.197390205C>A , CM000663.1:g.197390205C>A GRCh37
NC_000001.9:g.195656828C>A NCBI36
NG_008483.1:g.157798C>A
NG_008483.2:g.224614C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1247C>A MANE Select ENSP00000356370.3:p.Pro416His
ENST00000638467.1:c.1247C>A ENSP00000491102.1:p.Pro416His
ENST00000681519.1:c.128C>A ENSP00000505267.1:p.Pro43His
ENST00000367397.1:c.-611C>A ENSP00000356367.1:n.-611C>A
ENST00000367399.6:c.911C>A ENSP00000356369.2:p.Pro304His
ENST00000367400.7:c.1247C>A ENSP00000356370.3:p.Pro416His
ENST00000476483.1:n.207C>A
ENST00000484075.5:c.1247C>A ENSP00000433932.1:p.Pro416His
ENST00000535699.5:c.1040C>A ENSP00000438786.1:p.Pro347His
ENST00000538660.5:c.1247C>A ENSP00000438091.1:p.Pro416His
NM_001193640.1:c.911C>A NP_001180569.1:p.Pro304His
NM_001257965.1:c.1040C>A NP_001244894.1:p.Pro347His
NM_001257966.1:c.1247C>A NP_001244895.1:p.Pro416His
NM_201253.2:c.1247C>A NP_957705.1:p.Pro416His
NR_047563.1:n.1456C>A
NR_047564.1:n.1456C>A
XM_011509365.1:c.1247C>A XP_011507667.1:p.Pro416His
XM_011509366.1:c.1247C>A XP_011507668.1:p.Pro416His
XM_011509367.1:c.1247C>A XP_011507669.1:p.Pro416His
XM_011509368.1:c.665C>A XP_011507670.1:p.Pro222His
XM_011509369.1:c.-311C>A XP_011507671.1:n.-311C>A
XM_011509365.2:c.1247C>A XP_011507667.1:p.Pro416His
XM_011509369.2:c.-311C>A XP_011507671.1:n.-311C>A
XM_017000851.1:c.404C>A XP_016856340.1:p.Pro135His
XM_017000852.1:c.1247C>A XP_016856341.1:p.Pro416His
NM_201253.3:c.1247C>A MANE Select NP_957705.1:p.Pro416His
NM_001193640.2:c.911C>A NP_001180569.1:p.Pro304His
NM_001257965.2:c.1040C>A NP_001244894.1:p.Pro347His
NR_047563.2:n.1408C>A
NR_047564.2:n.1408C>A
NM_001257966.2:c.1247C>A NP_001244895.1:p.Pro416His