Canonical Allele Identifier: CA1311804
Community Standard Title: NM_201253.3(CRB1):c.1094G>A (p.Arg365His)
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197356936G>A , CM000663.2:g.197356936G>A GRCh38
NC_000001.10:g.197326066G>A , CM000663.1:g.197326066G>A GRCh37
NC_000001.9:g.195592689G>A NCBI36
NG_008483.1:g.93659G>A
NG_008483.2:g.160475G>A

Transcript Alleles

HGVS Amino-acid Change
NM_201253.3:c.1094G>A MANE Select NP_957705.1:p.Arg365His
ENST00000367400.8:c.1094G>A MANE Select ENSP00000356370.3:p.Arg365His
NM_001193640.1:c.758G>A NP_001180569.1:p.Arg253His
NM_001193640.2:c.758G>A NP_001180569.1:p.Arg253His
NM_001257965.1:c.887G>A NP_001244894.1:p.Arg296His
NM_001257965.2:c.887G>A NP_001244894.1:p.Arg296His
NM_001257966.1:c.1094G>A NP_001244895.1:p.Arg365His
NM_001257966.2:c.1094G>A NP_001244895.1:p.Arg365His
NM_201253.2:c.1094G>A NP_957705.1:p.Arg365His
NR_047563.1:n.1303G>A
NR_047563.2:n.1255G>A
NR_047564.1:n.1303G>A
NR_047564.2:n.1255G>A
ENST00000367399.6:c.758G>A ENSP00000356369.2:p.Arg253His
ENST00000367400.7:c.1094G>A ENSP00000356370.3:p.Arg365His
ENST00000475659.1:n.1231G>A
ENST00000484075.5:c.1094G>A ENSP00000433932.1:p.Arg365His
ENST00000535699.5:c.887G>A ENSP00000438786.1:p.Arg296His
ENST00000538660.5:c.1094G>A ENSP00000438091.1:p.Arg365His
ENST00000638467.1:c.1094G>A ENSP00000491102.1:p.Arg365His
XM_011509365.1:c.1094G>A XP_011507667.1:p.Arg365His
XM_011509365.2:c.1094G>A XP_011507667.1:p.Arg365His
XM_011509366.1:c.1094G>A XP_011507668.1:p.Arg365His
XM_011509367.1:c.1094G>A XP_011507669.1:p.Arg365His
XM_011509368.1:c.512G>A XP_011507670.1:p.Arg171His
XM_017000851.1:c.251G>A XP_016856340.1:p.Arg84His
XM_017000852.1:c.1094G>A XP_016856341.1:p.Arg365His