Canonical Allele Identifier: CA344031791
Gene: CRB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 801597
dbSNP Id: rs1571524102

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421461T>C , CM000663.2:g.197421461T>C GRCh38
NC_000001.10:g.197390591T>C , CM000663.1:g.197390591T>C GRCh37
NC_000001.9:g.195657214T>C NCBI36
NG_008483.1:g.158184T>C
NG_008483.2:g.225000T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1633T>C MANE Select ENSP00000356370.3:p.Ser545Pro
ENST00000638467.1:c.1633T>C ENSP00000491102.1:p.Ser545Pro
ENST00000681519.1:c.514T>C ENSP00000505267.1:p.Ser172Pro
ENST00000367397.1:c.-225T>C ENSP00000356367.1:n.-225T>C
ENST00000367399.6:c.1297T>C ENSP00000356369.2:p.Ser433Pro
ENST00000367400.7:c.1633T>C ENSP00000356370.3:p.Ser545Pro
ENST00000484075.5:c.1633T>C ENSP00000433932.1:p.Ser545Pro
ENST00000535699.5:c.1426T>C ENSP00000438786.1:p.Ser476Pro
ENST00000538660.5:c.1633T>C ENSP00000438091.1:p.Ser545Pro
NM_001193640.1:c.1297T>C NP_001180569.1:p.Ser433Pro
NM_001257965.1:c.1426T>C NP_001244894.1:p.Ser476Pro
NM_001257966.1:c.1633T>C NP_001244895.1:p.Ser545Pro
NM_201253.2:c.1633T>C NP_957705.1:p.Ser545Pro
NR_047563.1:n.1842T>C
NR_047564.1:n.1842T>C
XM_011509365.1:c.1633T>C XP_011507667.1:p.Ser545Pro
XM_011509366.1:c.1633T>C XP_011507668.1:p.Ser545Pro
XM_011509367.1:c.1633T>C XP_011507669.1:p.Ser545Pro
XM_011509368.1:c.1051T>C XP_011507670.1:p.Ser351Pro
XM_011509369.1:c.76T>C XP_011507671.1:p.Ser26Pro
XM_011509365.2:c.1633T>C XP_011507667.1:p.Ser545Pro
XM_011509369.2:c.76T>C XP_011507671.1:p.Ser26Pro
XM_017000851.1:c.790T>C XP_016856340.1:p.Ser264Pro
XM_017000852.1:c.1633T>C XP_016856341.1:p.Ser545Pro
NM_201253.3:c.1633T>C MANE Select NP_957705.1:p.Ser545Pro
NM_001193640.2:c.1297T>C NP_001180569.1:p.Ser433Pro
NM_001257965.2:c.1426T>C NP_001244894.1:p.Ser476Pro
NR_047563.2:n.1794T>C
NR_047564.2:n.1794T>C
NM_001257966.2:c.1633T>C NP_001244895.1:p.Ser545Pro