Canonical Allele Identifier: CA344032785
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197421693G>T , CM000663.2:g.197421693G>T GRCh38
NC_000001.10:g.197390823G>T , CM000663.1:g.197390823G>T GRCh37
NC_000001.9:g.195657446G>T NCBI36
NG_008483.1:g.158416G>T
NG_008483.2:g.225232G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.1865G>T MANE Select ENSP00000356370.3:p.Ser622Ile
ENST00000638467.1:c.1865G>T ENSP00000491102.1:p.Ser622Ile
ENST00000681519.1:c.746G>T ENSP00000505267.1:p.Ser249Ile
ENST00000367397.1:c.8G>T ENSP00000356367.1:p.Ser3Ile
ENST00000367399.6:c.1529G>T ENSP00000356369.2:p.Ser510Ile
ENST00000367400.7:c.1865G>T ENSP00000356370.3:p.Ser622Ile
ENST00000484075.5:c.1865G>T ENSP00000433932.1:p.Ser622Ile
ENST00000535699.5:c.1658G>T ENSP00000438786.1:p.Ser553Ile
ENST00000538660.5:c.1865G>T ENSP00000438091.1:p.Ser622Ile
NM_001193640.1:c.1529G>T NP_001180569.1:p.Ser510Ile
NM_001257965.1:c.1658G>T NP_001244894.1:p.Ser553Ile
NM_001257966.1:c.1865G>T NP_001244895.1:p.Ser622Ile
NM_201253.2:c.1865G>T NP_957705.1:p.Ser622Ile
NR_047563.1:n.1923-57G>T
NR_047564.1:n.2074G>T
XM_011509365.1:c.1865G>T XP_011507667.1:p.Ser622Ile
XM_011509366.1:c.1865G>T XP_011507668.1:p.Ser622Ile
XM_011509367.1:c.1865G>T XP_011507669.1:p.Ser622Ile
XM_011509368.1:c.1283G>T XP_011507670.1:p.Ser428Ile
XM_011509369.1:c.308G>T XP_011507671.1:p.Ser103Ile
XM_011509365.2:c.1865G>T XP_011507667.1:p.Ser622Ile
XM_011509369.2:c.308G>T XP_011507671.1:p.Ser103Ile
XM_017000851.1:c.1022G>T XP_016856340.1:p.Ser341Ile
XM_017000852.1:c.1865G>T XP_016856341.1:p.Ser622Ile
NM_201253.3:c.1865G>T MANE Select NP_957705.1:p.Ser622Ile
NM_001193640.2:c.1529G>T NP_001180569.1:p.Ser510Ile
NM_001257965.2:c.1658G>T NP_001244894.1:p.Ser553Ile
NR_047563.2:n.1875-57G>T
NR_047564.2:n.2026G>T
NM_001257966.2:c.1865G>T NP_001244895.1:p.Ser622Ile