Canonical Allele Identifier: CA1312380
Community Standard Title: NM_201253.3(CRB1):c.3712T>C (p.Cys1238Arg)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197435575T>C , CM000663.2:g.197435575T>C GRCh38
NC_000001.10:g.197404705T>C , CM000663.1:g.197404705T>C GRCh37
NC_000001.9:g.195671328T>C NCBI36
NG_008483.1:g.172298T>C
NG_008483.2:g.239114T>C

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.3712T>C MANE Select NP_957705.1:p.Cys1238Arg
ENST00000367400.8:c.3712T>C MANE Select ENSP00000356370.3:p.Cys1238Arg
NM_001193640.1:c.3376T>C NP_001180569.1:p.Cys1126Arg
NM_001193640.2:c.3376T>C NP_001180569.1:p.Cys1126Arg
NM_001257965.1:c.3640T>C NP_001244894.1:p.Cys1214Arg
NM_001257965.2:c.3640T>C NP_001244894.1:p.Cys1214Arg
NM_001257966.1:c.2129-25T>C NP_001244895.1:n.2129-25T>C
NM_001257966.2:c.2129-25T>C NP_001244895.1:n.2129-25T>C
NM_201253.2:c.3712T>C NP_957705.1:p.Cys1238Arg
NR_047563.1:n.3713T>C
NR_047563.2:n.3665T>C
NR_047564.1:n.3921T>C
NR_047564.2:n.3873T>C
ENST00000367397.1:c.1855T>C ENSP00000356367.1:p.Cys619Arg
ENST00000367399.6:c.3376T>C ENSP00000356369.2:p.Cys1126Arg
ENST00000367400.7:c.3712T>C ENSP00000356370.3:p.Cys1238Arg
ENST00000484075.5:c.3712T>C ENSP00000433932.1:p.Cys1238Arg
ENST00000535699.5:c.3640T>C ENSP00000438786.1:p.Cys1214Arg
ENST00000538660.5:c.2129-25T>C ENSP00000438091.1:n.2129-25T>C
ENST00000638467.1:c.3712T>C ENSP00000491102.1:p.Cys1238Arg
ENST00000681519.1:c.2593T>C ENSP00000505267.1:p.Cys865Arg
XM_011509365.1:c.3712T>C XP_011507667.1:p.Cys1238Arg
XM_011509365.2:c.3712T>C XP_011507667.1:p.Cys1238Arg
XM_011509366.1:c.3712T>C XP_011507668.1:p.Cys1238Arg
XM_011509367.1:c.3712T>C XP_011507669.1:p.Cys1238Arg
XM_011509368.1:c.3130T>C XP_011507670.1:p.Cys1044Arg
XM_011509369.1:c.2155T>C XP_011507671.1:p.Cys719Arg
XM_011509369.2:c.2155T>C XP_011507671.1:p.Cys719Arg
XM_017000851.1:c.2869T>C XP_016856340.1:p.Cys957Arg
XM_017000852.1:c.3847T>C XP_016856341.1:p.Cys1283Arg