Canonical Allele Identifier: CA344084973
Community Standard Title: NM_201253.3(CRB1):c.80G>T (p.Cys27Phe)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197328431G>T , CM000663.2:g.197328431G>T GRCh38
NC_000001.10:g.197297561G>T , CM000663.1:g.197297561G>T GRCh37
NC_000001.9:g.195564184G>T NCBI36
NG_008483.1:g.65154G>T
NG_008483.2:g.131970G>T

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.80G>T MANE Select NP_957705.1:p.Cys27Phe
ENST00000367400.8:c.80G>T MANE Select ENSP00000356370.3:p.Cys27Phe
NM_001193640.1:c.80G>T NP_001180569.1:p.Cys27Phe
NM_001193640.2:c.80G>T NP_001180569.1:p.Cys27Phe
NM_001257965.1:c.-128G>T NP_001244894.1:n.-128G>T
NM_001257965.2:c.-128G>T NP_001244894.1:n.-128G>T
NM_001257966.1:c.80G>T NP_001244895.1:p.Cys27Phe
NM_001257966.2:c.80G>T NP_001244895.1:p.Cys27Phe
NM_201253.2:c.80G>T NP_957705.1:p.Cys27Phe
NR_047563.1:n.289G>T
NR_047563.2:n.241G>T
NR_047564.1:n.289G>T
NR_047564.2:n.241G>T
ENST00000367399.6:c.80G>T ENSP00000356369.2:p.Cys27Phe
ENST00000367400.7:c.80G>T ENSP00000356370.3:p.Cys27Phe
ENST00000475659.1:n.217G>T
ENST00000484075.5:c.80G>T ENSP00000433932.1:p.Cys27Phe
ENST00000535699.5:c.-128G>T ENSP00000438786.1:n.-128G>T
ENST00000538660.5:c.80G>T ENSP00000438091.1:p.Cys27Phe
ENST00000638467.1:c.80G>T ENSP00000491102.1:p.Cys27Phe
XM_011509365.1:c.80G>T XP_011507667.1:p.Cys27Phe
XM_011509365.2:c.80G>T XP_011507667.1:p.Cys27Phe
XM_011509366.1:c.80G>T XP_011507668.1:p.Cys27Phe
XM_011509367.1:c.80G>T XP_011507669.1:p.Cys27Phe
XM_011509368.1:c.71-15850G>T XP_011507670.1:n.71-15850G>T
XM_017000851.1:c.-624G>T XP_016856340.1:n.-624G>T
XM_017000852.1:c.80G>T XP_016856341.1:p.Cys27Phe