Canonical Allele Identifier: CA344085013
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328448A>G , CM000663.2:g.197328448A>G GRCh38
NC_000001.10:g.197297578A>G , CM000663.1:g.197297578A>G GRCh37
NC_000001.9:g.195564201A>G NCBI36
NG_008483.1:g.65171A>G
NG_008483.2:g.131987A>G

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.97A>G MANE Select NP_957705.1:p.Arg33Gly
ENST00000367400.8:c.97A>G MANE Select ENSP00000356370.3:p.Arg33Gly
NM_001193640.1:c.97A>G NP_001180569.1:p.Arg33Gly
NM_001193640.2:c.97A>G NP_001180569.1:p.Arg33Gly
NM_001257965.1:c.-111A>G NP_001244894.1:n.-111A>G
NM_001257965.2:c.-111A>G NP_001244894.1:n.-111A>G
NM_001257966.1:c.97A>G NP_001244895.1:p.Arg33Gly
NM_001257966.2:c.97A>G NP_001244895.1:p.Arg33Gly
NM_201253.2:c.97A>G NP_957705.1:p.Arg33Gly
NR_047563.1:n.306A>G
NR_047563.2:n.258A>G
NR_047564.1:n.306A>G
NR_047564.2:n.258A>G
ENST00000367399.6:c.97A>G ENSP00000356369.2:p.Arg33Gly
ENST00000367400.7:c.97A>G ENSP00000356370.3:p.Arg33Gly
ENST00000475659.1:n.234A>G
ENST00000484075.5:c.97A>G ENSP00000433932.1:p.Arg33Gly
ENST00000535699.5:c.-111A>G ENSP00000438786.1:n.-111A>G
ENST00000538660.5:c.97A>G ENSP00000438091.1:p.Arg33Gly
ENST00000638467.1:c.97A>G ENSP00000491102.1:p.Arg33Gly
XM_011509365.1:c.97A>G XP_011507667.1:p.Arg33Gly
XM_011509365.2:c.97A>G XP_011507667.1:p.Arg33Gly
XM_011509366.1:c.97A>G XP_011507668.1:p.Arg33Gly
XM_011509367.1:c.97A>G XP_011507669.1:p.Arg33Gly
XM_011509368.1:c.71-15833A>G XP_011507670.1:n.71-15833A>G
XM_017000851.1:c.-607A>G XP_016856340.1:n.-607A>G
XM_017000852.1:c.97A>G XP_016856341.1:p.Arg33Gly