Canonical Allele Identifier: CA344046524
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435053A>C , CM000663.2:g.197435053A>C GRCh38
NC_000001.10:g.197404183A>C , CM000663.1:g.197404183A>C GRCh37
NC_000001.9:g.195670806A>C NCBI36
NG_008483.1:g.171776A>C
NG_008483.2:g.238592A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.3190A>C MANE Select ENSP00000356370.3:p.Ser1064Arg
ENST00000638467.1:c.3190A>C ENSP00000491102.1:p.Ser1064Arg
ENST00000681519.1:c.2071A>C ENSP00000505267.1:p.Ser691Arg
ENST00000367397.1:c.1333A>C ENSP00000356367.1:p.Ser445Arg
ENST00000367399.6:c.2854A>C ENSP00000356369.2:p.Ser952Arg
ENST00000367400.7:c.3190A>C ENSP00000356370.3:p.Ser1064Arg
ENST00000484075.5:c.3190A>C ENSP00000433932.1:p.Ser1064Arg
ENST00000535699.5:c.3118A>C ENSP00000438786.1:p.Ser1040Arg
ENST00000538660.5:c.2129-547A>C ENSP00000438091.1:n.2129-547A>C
NM_001193640.1:c.2854A>C NP_001180569.1:p.Ser952Arg
NM_001257965.1:c.3118A>C NP_001244894.1:p.Ser1040Arg
NM_001257966.1:c.2129-547A>C NP_001244895.1:n.2129-547A>C
NM_201253.2:c.3190A>C NP_957705.1:p.Ser1064Arg
NR_047563.1:n.3191A>C
NR_047564.1:n.3399A>C
XM_011509365.1:c.3190A>C XP_011507667.1:p.Ser1064Arg
XM_011509366.1:c.3190A>C XP_011507668.1:p.Ser1064Arg
XM_011509367.1:c.3190A>C XP_011507669.1:p.Ser1064Arg
XM_011509368.1:c.2608A>C XP_011507670.1:p.Ser870Arg
XM_011509369.1:c.1633A>C XP_011507671.1:p.Ser545Arg
XM_011509365.2:c.3190A>C XP_011507667.1:p.Ser1064Arg
XM_011509369.2:c.1633A>C XP_011507671.1:p.Ser545Arg
XM_017000851.1:c.2347A>C XP_016856340.1:p.Ser783Arg
XM_017000852.1:c.3325A>C XP_016856341.1:p.Ser1109Arg
NM_201253.3:c.3190A>C MANE Select NP_957705.1:p.Ser1064Arg
NM_001193640.2:c.2854A>C NP_001180569.1:p.Ser952Arg
NM_001257965.2:c.3118A>C NP_001244894.1:p.Ser1040Arg
NR_047563.2:n.3143A>C
NR_047564.2:n.3351A>C
NM_001257966.2:c.2129-547A>C NP_001244895.1:n.2129-547A>C