Canonical Allele Identifier: CA1312065
Community Standard Title: NM_201253.3(CRB1):c.2171A>G (p.Tyr724Cys)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197427496A>G , CM000663.2:g.197427496A>G GRCh38
NC_000001.10:g.197396626A>G , CM000663.1:g.197396626A>G GRCh37
NC_000001.9:g.195663249A>G NCBI36
NG_008483.1:g.164219A>G
NG_008483.2:g.231035A>G

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.2171A>G MANE Select NP_957705.1:p.Tyr724Cys
ENST00000367400.8:c.2171A>G MANE Select ENSP00000356370.3:p.Tyr724Cys
NM_001193640.1:c.1835A>G NP_001180569.1:p.Tyr612Cys
NM_001193640.2:c.1835A>G NP_001180569.1:p.Tyr612Cys
NM_001257965.1:c.1964A>G NP_001244894.1:p.Tyr655Cys
NM_001257965.2:c.1964A>G NP_001244894.1:p.Tyr655Cys
NM_001257966.1:c.2128+5540A>G NP_001244895.1:n.2128+5540A>G
NM_001257966.2:c.2128+5540A>G NP_001244895.1:n.2128+5540A>G
NM_201253.2:c.2171A>G NP_957705.1:p.Tyr724Cys
NR_047563.1:n.2172A>G
NR_047563.2:n.2124A>G
NR_047564.1:n.2380A>G
NR_047564.2:n.2332A>G
ENST00000367397.1:c.314A>G ENSP00000356367.1:p.Tyr105Cys
ENST00000367399.6:c.1835A>G ENSP00000356369.2:p.Tyr612Cys
ENST00000367400.7:c.2171A>G ENSP00000356370.3:p.Tyr724Cys
ENST00000480086.2:n.72A>G
ENST00000484075.5:c.2171A>G ENSP00000433932.1:p.Tyr724Cys
ENST00000535699.5:c.1964A>G ENSP00000438786.1:p.Tyr655Cys
ENST00000538660.5:c.2128+5540A>G ENSP00000438091.1:n.2128+5540A>G
ENST00000638467.1:c.2171A>G ENSP00000491102.1:p.Tyr724Cys
ENST00000681519.1:c.1052A>G ENSP00000505267.1:p.Tyr351Cys
XM_011509365.1:c.2171A>G XP_011507667.1:p.Tyr724Cys
XM_011509365.2:c.2171A>G XP_011507667.1:p.Tyr724Cys
XM_011509366.1:c.2171A>G XP_011507668.1:p.Tyr724Cys
XM_011509367.1:c.2171A>G XP_011507669.1:p.Tyr724Cys
XM_011509368.1:c.1589A>G XP_011507670.1:p.Tyr530Cys
XM_011509369.1:c.614A>G XP_011507671.1:p.Tyr205Cys
XM_011509369.2:c.614A>G XP_011507671.1:p.Tyr205Cys
XM_017000851.1:c.1328A>G XP_016856340.1:p.Tyr443Cys
XM_017000852.1:c.2171A>G XP_016856341.1:p.Tyr724Cys