Canonical Allele Identifier: CA344036948

Gene: CRB1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427637G>A , CM000663.2:g.197427637G>A	GRCh38
NC_000001.10:g.197396767G>A , CM000663.1:g.197396767G>A	GRCh37
NC_000001.9:g.195663390G>A	NCBI36
NG_008483.1:g.164360G>A
NG_008483.2:g.231176G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2312G>A MANE Select	ENSP00000356370.3:p.Arg771Lys
ENST00000638467.1:c.2312G>A	ENSP00000491102.1:p.Arg771Lys
ENST00000681519.1:c.1193G>A	ENSP00000505267.1:p.Arg398Lys
ENST00000367397.1:c.455G>A	ENSP00000356367.1:p.Arg152Lys
ENST00000367399.6:c.1976G>A	ENSP00000356369.2:p.Arg659Lys
ENST00000367400.7:c.2312G>A	ENSP00000356370.3:p.Arg771Lys
ENST00000480086.2:n.213G>A
ENST00000484075.5:c.2312G>A	ENSP00000433932.1:p.Arg771Lys
ENST00000535699.5:c.2105G>A	ENSP00000438786.1:p.Arg702Lys
ENST00000538660.5:c.2128+5681G>A	ENSP00000438091.1:n.2128+5681G>A
NM_001193640.1:c.1976G>A	NP_001180569.1:p.Arg659Lys
NM_001257965.1:c.2105G>A	NP_001244894.1:p.Arg702Lys
NM_001257966.1:c.2128+5681G>A	NP_001244895.1:n.2128+5681G>A
NM_201253.2:c.2312G>A	NP_957705.1:p.Arg771Lys
NR_047563.1:n.2313G>A
NR_047564.1:n.2521G>A
XM_011509365.1:c.2312G>A	XP_011507667.1:p.Arg771Lys
XM_011509366.1:c.2312G>A	XP_011507668.1:p.Arg771Lys
XM_011509367.1:c.2312G>A	XP_011507669.1:p.Arg771Lys
XM_011509368.1:c.1730G>A	XP_011507670.1:p.Arg577Lys
XM_011509369.1:c.755G>A	XP_011507671.1:p.Arg252Lys
XM_011509365.2:c.2312G>A	XP_011507667.1:p.Arg771Lys
XM_011509369.2:c.755G>A	XP_011507671.1:p.Arg252Lys
XM_017000851.1:c.1469G>A	XP_016856340.1:p.Arg490Lys
XM_017000852.1:c.2312G>A	XP_016856341.1:p.Arg771Lys
NM_201253.3:c.2312G>A MANE Select	NP_957705.1:p.Arg771Lys
NM_001193640.2:c.1976G>A	NP_001180569.1:p.Arg659Lys
NM_001257965.2:c.2105G>A	NP_001244894.1:p.Arg702Lys
NR_047563.2:n.2265G>A
NR_047564.2:n.2473G>A
NM_001257966.2:c.2128+5681G>A	NP_001244895.1:n.2128+5681G>A