Canonical Allele Identifier: CA344085592
Community Standard Title: NM_201253.3(CRB1):c.358C>T (p.Gln120Ter)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328709C>T , CM000663.2:g.197328709C>T GRCh38
NC_000001.10:g.197297839C>T , CM000663.1:g.197297839C>T GRCh37
NC_000001.9:g.195564462C>T NCBI36
NG_008483.1:g.65432C>T
NG_008483.2:g.132248C>T

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.358C>T MANE Select NP_957705.1:p.Gln120Ter
ENST00000367400.8:c.358C>T MANE Select ENSP00000356370.3:p.Gln120Ter
NM_001193640.1:c.358C>T NP_001180569.1:p.Gln120Ter
NM_001193640.2:c.358C>T NP_001180569.1:p.Gln120Ter
NM_001257965.1:c.151C>T NP_001244894.1:p.Gln51Ter
NM_001257965.2:c.151C>T NP_001244894.1:p.Gln51Ter
NM_001257966.1:c.358C>T NP_001244895.1:p.Gln120Ter
NM_001257966.2:c.358C>T NP_001244895.1:p.Gln120Ter
NM_201253.2:c.358C>T NP_957705.1:p.Gln120Ter
NR_047563.1:n.567C>T
NR_047563.2:n.519C>T
NR_047564.1:n.567C>T
NR_047564.2:n.519C>T
ENST00000367399.6:c.358C>T ENSP00000356369.2:p.Gln120Ter
ENST00000367400.7:c.358C>T ENSP00000356370.3:p.Gln120Ter
ENST00000475659.1:n.495C>T
ENST00000484075.5:c.358C>T ENSP00000433932.1:p.Gln120Ter
ENST00000535699.5:c.151C>T ENSP00000438786.1:p.Gln51Ter
ENST00000538660.5:c.358C>T ENSP00000438091.1:p.Gln120Ter
ENST00000638467.1:c.358C>T ENSP00000491102.1:p.Gln120Ter
XM_011509365.1:c.358C>T XP_011507667.1:p.Gln120Ter
XM_011509365.2:c.358C>T XP_011507667.1:p.Gln120Ter
XM_011509366.1:c.358C>T XP_011507668.1:p.Gln120Ter
XM_011509367.1:c.358C>T XP_011507669.1:p.Gln120Ter
XM_011509368.1:c.71-15572C>T XP_011507670.1:n.71-15572C>T
XM_017000851.1:c.-346C>T XP_016856340.1:n.-346C>T
XM_017000852.1:c.358C>T XP_016856341.1:p.Gln120Ter