Canonical Allele Identifier: CA344050252
Community Standard Title: NM_201253.3(CRB1):c.3653G>T (p.Cys1218Phe)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435516G>T , CM000663.2:g.197435516G>T GRCh38
NC_000001.10:g.197404646G>T , CM000663.1:g.197404646G>T GRCh37
NC_000001.9:g.195671269G>T NCBI36
NG_008483.1:g.172239G>T
NG_008483.2:g.239055G>T

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.3653G>T MANE Select NP_957705.1:p.Cys1218Phe
ENST00000367400.8:c.3653G>T MANE Select ENSP00000356370.3:p.Cys1218Phe
NM_001193640.1:c.3317G>T NP_001180569.1:p.Cys1106Phe
NM_001193640.2:c.3317G>T NP_001180569.1:p.Cys1106Phe
NM_001257965.1:c.3581G>T NP_001244894.1:p.Cys1194Phe
NM_001257965.2:c.3581G>T NP_001244894.1:p.Cys1194Phe
NM_001257966.1:c.2129-84G>T NP_001244895.1:n.2129-84G>T
NM_001257966.2:c.2129-84G>T NP_001244895.1:n.2129-84G>T
NM_201253.2:c.3653G>T NP_957705.1:p.Cys1218Phe
NR_047563.1:n.3654G>T
NR_047563.2:n.3606G>T
NR_047564.1:n.3862G>T
NR_047564.2:n.3814G>T
ENST00000367397.1:c.1796G>T ENSP00000356367.1:p.Cys599Phe
ENST00000367399.6:c.3317G>T ENSP00000356369.2:p.Cys1106Phe
ENST00000367400.7:c.3653G>T ENSP00000356370.3:p.Cys1218Phe
ENST00000484075.5:c.3653G>T ENSP00000433932.1:p.Cys1218Phe
ENST00000535699.5:c.3581G>T ENSP00000438786.1:p.Cys1194Phe
ENST00000538660.5:c.2129-84G>T ENSP00000438091.1:n.2129-84G>T
ENST00000638467.1:c.3653G>T ENSP00000491102.1:p.Cys1218Phe
ENST00000681519.1:c.2534G>T ENSP00000505267.1:p.Cys845Phe
XM_011509365.1:c.3653G>T XP_011507667.1:p.Cys1218Phe
XM_011509365.2:c.3653G>T XP_011507667.1:p.Cys1218Phe
XM_011509366.1:c.3653G>T XP_011507668.1:p.Cys1218Phe
XM_011509367.1:c.3653G>T XP_011507669.1:p.Cys1218Phe
XM_011509368.1:c.3071G>T XP_011507670.1:p.Cys1024Phe
XM_011509369.1:c.2096G>T XP_011507671.1:p.Cys699Phe
XM_011509369.2:c.2096G>T XP_011507671.1:p.Cys699Phe
XM_017000851.1:c.2810G>T XP_016856340.1:p.Cys937Phe
XM_017000852.1:c.3788G>T XP_016856341.1:p.Cys1263Phe