Canonical Allele Identifier: CA344081625
Gene: CRB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328942C>A , CM000663.2:g.197328942C>A GRCh38
NC_000001.10:g.197298072C>A , CM000663.1:g.197298072C>A GRCh37
NC_000001.9:g.195564695C>A NCBI36
NG_008483.1:g.65665C>A
NG_008483.2:g.132481C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.591C>A MANE Select ENSP00000356370.3:p.Asn197Lys
ENST00000638467.1:c.591C>A ENSP00000491102.1:p.Asn197Lys
ENST00000367399.6:c.591C>A ENSP00000356369.2:p.Asn197Lys
ENST00000367400.7:c.591C>A ENSP00000356370.3:p.Asn197Lys
ENST00000475659.1:n.728C>A
ENST00000484075.5:c.591C>A ENSP00000433932.1:p.Asn197Lys
ENST00000535699.5:c.384C>A ENSP00000438786.1:p.Asn128Lys
ENST00000538660.5:c.591C>A ENSP00000438091.1:p.Asn197Lys
NM_001193640.1:c.591C>A NP_001180569.1:p.Asn197Lys
NM_001257965.1:c.384C>A NP_001244894.1:p.Asn128Lys
NM_001257966.1:c.591C>A NP_001244895.1:p.Asn197Lys
NM_201253.2:c.591C>A NP_957705.1:p.Asn197Lys
NR_047563.1:n.800C>A
NR_047564.1:n.800C>A
XM_011509365.1:c.591C>A XP_011507667.1:p.Asn197Lys
XM_011509366.1:c.591C>A XP_011507668.1:p.Asn197Lys
XM_011509367.1:c.591C>A XP_011507669.1:p.Asn197Lys
XM_011509368.1:c.71-15339C>A XP_011507670.1:n.71-15339C>A
XM_011509365.2:c.591C>A XP_011507667.1:p.Asn197Lys
XM_017000851.1:c.-113C>A XP_016856340.1:n.-113C>A
XM_017000852.1:c.591C>A XP_016856341.1:p.Asn197Lys
NM_201253.3:c.591C>A MANE Select NP_957705.1:p.Asn197Lys
NM_001193640.2:c.591C>A NP_001180569.1:p.Asn197Lys
NM_001257965.2:c.384C>A NP_001244894.1:p.Asn128Lys
NR_047563.2:n.752C>A
NR_047564.2:n.752C>A
NM_001257966.2:c.591C>A NP_001244895.1:p.Asn197Lys