Canonical Allele Identifier: CA344035912

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446963A>T (hg19) ; chr1:g.197477833A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477833A>T , CM000663.2:g.197477833A>T	GRCh38
NC_000001.10:g.197446963A>T , CM000663.1:g.197446963A>T	GRCh37
NC_000001.9:g.195713586A>T	NCBI36
NG_008483.1:g.214556A>T
NG_008483.2:g.281372A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4175A>T MANE Select	ENSP00000356370.3:p.Glu1392Val
ENST00000367399.6:c.3839A>T	ENSP00000356369.2:p.Glu1280Val
ENST00000367400.7:c.4175A>T	ENSP00000356370.3:p.Glu1392Val
ENST00000448952.1:c.409A>T	ENSP00000395407.1:n.409A>T
ENST00000484075.5:c.*286A>T	ENSP00000433932.1:n.*286A>T
ENST00000535699.5:c.4103A>T	ENSP00000438786.1:p.Glu1368Val
ENST00000538660.5:c.2567A>T	ENSP00000438091.1:p.Glu856Val
NM_001193640.1:c.3839A>T	NP_001180569.1:p.Glu1280Val
NM_001257965.1:c.4103A>T	NP_001244894.1:p.Glu1368Val
NM_001257966.1:c.2567A>T	NP_001244895.1:p.Glu856Val
NM_201253.2:c.4175A>T	NP_957705.1:p.Glu1392Val
NR_047563.1:n.4176A>T
NR_047564.1:n.4626A>T
XM_011509366.1:c.*280A>T	XP_011507668.1:n.*280A>T
XM_011509367.1:c.*154A>T	XP_011507669.1:n.*154A>T
XM_011509368.1:c.3593A>T	XP_011507670.1:p.Glu1198Val
XM_011509369.1:c.2618A>T	XP_011507671.1:p.Glu873Val
XM_011509369.2:c.2618A>T	XP_011507671.1:p.Glu873Val
XM_017000851.1:c.3332A>T	XP_016856340.1:p.Glu1111Val
XM_017000852.1:c.4310A>T	XP_016856341.1:p.Glu1437Val
NM_201253.3:c.4175A>T MANE Select	NP_957705.1:p.Glu1392Val
NM_001193640.2:c.3839A>T	NP_001180569.1:p.Glu1280Val
NM_001257965.2:c.4103A>T	NP_001244894.1:p.Glu1368Val
NR_047563.2:n.4128A>T
NR_047564.2:n.4578A>T
NM_001257966.2:c.2567A>T	NP_001244895.1:p.Glu856Val