Canonical Allele Identifier: CA2574105565
Gene: CRB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197429369_197429370insG , CM000663.2:g.197429369_197429370insG GRCh38
NC_000001.10:g.197398499_197398500insG , CM000663.1:g.197398499_197398500insG GRCh37
NC_000001.9:g.195665122_195665123insG NCBI36
NG_008483.1:g.166092_166093insG
NG_008483.2:g.232908_232909insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367400.8:c.2677-80_2677-79insG MANE Select ENSP00000356370.3:n.2677-80_2677-79insG
ENST00000638467.1:c.2677-80_2677-79insG ENSP00000491102.1:n.2677-80_2677-79insG
ENST00000681519.1:c.1558-80_1558-79insG ENSP00000505267.1:n.1558-80_1558-79insG
ENST00000367397.1:c.820-80_820-79insG ENSP00000356367.1:n.820-80_820-79insG
ENST00000367399.6:c.2341-80_2341-79insG ENSP00000356369.2:n.2341-80_2341-79insG
ENST00000367400.7:c.2677-80_2677-79insG ENSP00000356370.3:n.2677-80_2677-79insG
ENST00000484075.5:c.2677-80_2677-79insG ENSP00000433932.1:n.2677-80_2677-79insG
ENST00000535699.5:c.2605-80_2605-79insG ENSP00000438786.1:n.2605-80_2605-79insG
ENST00000538660.5:c.2129-6231_2129-6230insG ENSP00000438091.1:n.2129-6231_2129-6230insG
NM_001193640.1:c.2341-80_2341-79insG NP_001180569.1:n.2341-80_2341-79insG
NM_001257965.1:c.2605-80_2605-79insG NP_001244894.1:n.2605-80_2605-79insG
NM_001257966.1:c.2129-6231_2129-6230insG NP_001244895.1:n.2129-6231_2129-6230insG
NM_201253.2:c.2677-80_2677-79insG NP_957705.1:n.2677-80_2677-79insG
NR_047563.1:n.2678-80_2678-79insG
NR_047564.1:n.2886-80_2886-79insG
XM_011509365.1:c.2677-80_2677-79insG XP_011507667.1:n.2677-80_2677-79insG
XM_011509366.1:c.2677-80_2677-79insG XP_011507668.1:n.2677-80_2677-79insG
XM_011509367.1:c.2677-80_2677-79insG XP_011507669.1:n.2677-80_2677-79insG
XM_011509368.1:c.2095-80_2095-79insG XP_011507670.1:n.2095-80_2095-79insG
XM_011509369.1:c.1120-80_1120-79insG XP_011507671.1:n.1120-80_1120-79insG
XM_011509365.2:c.2677-80_2677-79insG XP_011507667.1:n.2677-80_2677-79insG
XM_011509369.2:c.1120-80_1120-79insG XP_011507671.1:n.1120-80_1120-79insG
XM_017000851.1:c.1834-80_1834-79insG XP_016856340.1:n.1834-80_1834-79insG
XM_017000852.1:c.2812-80_2812-79insG XP_016856341.1:n.2812-80_2812-79insG
NM_201253.3:c.2677-80_2677-79insG MANE Select NP_957705.1:n.2677-80_2677-79insG
NM_001193640.2:c.2341-80_2341-79insG NP_001180569.1:n.2341-80_2341-79insG
NM_001257965.2:c.2605-80_2605-79insG NP_001244894.1:n.2605-80_2605-79insG
NR_047563.2:n.2630-80_2630-79insG
NR_047564.2:n.2838-80_2838-79insG
NM_001257966.2:c.2129-6231_2129-6230insG NP_001244895.1:n.2129-6231_2129-6230insG