Canonical Allele Identifier: CA344084970
Gene: CRB1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328430T>A , CM000663.2:g.197328430T>A GRCh38
NC_000001.10:g.197297560T>A , CM000663.1:g.197297560T>A GRCh37
NC_000001.9:g.195564183T>A NCBI36
NG_008483.1:g.65153T>A
NG_008483.2:g.131969T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.79T>A MANE Select ENSP00000356370.3:p.Cys27Ser
ENST00000638467.1:c.79T>A ENSP00000491102.1:p.Cys27Ser
ENST00000367399.6:c.79T>A ENSP00000356369.2:p.Cys27Ser
ENST00000367400.7:c.79T>A ENSP00000356370.3:p.Cys27Ser
ENST00000475659.1:n.216T>A
ENST00000484075.5:c.79T>A ENSP00000433932.1:p.Cys27Ser
ENST00000535699.5:c.-129T>A ENSP00000438786.1:n.-129T>A
ENST00000538660.5:c.79T>A ENSP00000438091.1:p.Cys27Ser
NM_001193640.1:c.79T>A NP_001180569.1:p.Cys27Ser
NM_001257965.1:c.-129T>A NP_001244894.1:n.-129T>A
NM_001257966.1:c.79T>A NP_001244895.1:p.Cys27Ser
NM_201253.2:c.79T>A NP_957705.1:p.Cys27Ser
NR_047563.1:n.288T>A
NR_047564.1:n.288T>A
XM_011509365.1:c.79T>A XP_011507667.1:p.Cys27Ser
XM_011509366.1:c.79T>A XP_011507668.1:p.Cys27Ser
XM_011509367.1:c.79T>A XP_011507669.1:p.Cys27Ser
XM_011509368.1:c.71-15851T>A XP_011507670.1:n.71-15851T>A
XM_011509365.2:c.79T>A XP_011507667.1:p.Cys27Ser
XM_017000851.1:c.-625T>A XP_016856340.1:n.-625T>A
XM_017000852.1:c.79T>A XP_016856341.1:p.Cys27Ser
NM_201253.3:c.79T>A MANE Select NP_957705.1:p.Cys27Ser
NM_001193640.2:c.79T>A NP_001180569.1:p.Cys27Ser
NM_001257965.2:c.-129T>A NP_001244894.1:n.-129T>A
NR_047563.2:n.240T>A
NR_047564.2:n.240T>A
NM_001257966.2:c.79T>A NP_001244895.1:p.Cys27Ser