Canonical Allele Identifier: CA344085889
Community Standard Title: NM_201253.3(CRB1):c.490C>T (p.Gln164Ter)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328841C>T , CM000663.2:g.197328841C>T GRCh38
NC_000001.10:g.197297971C>T , CM000663.1:g.197297971C>T GRCh37
NC_000001.9:g.195564594C>T NCBI36
NG_008483.1:g.65564C>T
NG_008483.2:g.132380C>T

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.490C>T MANE Select NP_957705.1:p.Gln164Ter
ENST00000367400.8:c.490C>T MANE Select ENSP00000356370.3:p.Gln164Ter
NM_001193640.1:c.490C>T NP_001180569.1:p.Gln164Ter
NM_001193640.2:c.490C>T NP_001180569.1:p.Gln164Ter
NM_001257965.1:c.283C>T NP_001244894.1:p.Gln95Ter
NM_001257965.2:c.283C>T NP_001244894.1:p.Gln95Ter
NM_001257966.1:c.490C>T NP_001244895.1:p.Gln164Ter
NM_001257966.2:c.490C>T NP_001244895.1:p.Gln164Ter
NM_201253.2:c.490C>T NP_957705.1:p.Gln164Ter
NR_047563.1:n.699C>T
NR_047563.2:n.651C>T
NR_047564.1:n.699C>T
NR_047564.2:n.651C>T
ENST00000367399.6:c.490C>T ENSP00000356369.2:p.Gln164Ter
ENST00000367400.7:c.490C>T ENSP00000356370.3:p.Gln164Ter
ENST00000475659.1:n.627C>T
ENST00000484075.5:c.490C>T ENSP00000433932.1:p.Gln164Ter
ENST00000535699.5:c.283C>T ENSP00000438786.1:p.Gln95Ter
ENST00000538660.5:c.490C>T ENSP00000438091.1:p.Gln164Ter
ENST00000638467.1:c.490C>T ENSP00000491102.1:p.Gln164Ter
XM_011509365.1:c.490C>T XP_011507667.1:p.Gln164Ter
XM_011509365.2:c.490C>T XP_011507667.1:p.Gln164Ter
XM_011509366.1:c.490C>T XP_011507668.1:p.Gln164Ter
XM_011509367.1:c.490C>T XP_011507669.1:p.Gln164Ter
XM_011509368.1:c.71-15440C>T XP_011507670.1:n.71-15440C>T
XM_017000851.1:c.-214C>T XP_016856340.1:n.-214C>T
XM_017000852.1:c.490C>T XP_016856341.1:p.Gln164Ter