Canonical Allele Identifier: CA1218066457

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427902C= , CM000663.2:g.197427902C=	GRCh38
NC_000001.10:g.197397032C= , CM000663.1:g.197397032C=	GRCh37
NC_000001.9:g.195663655C=	NCBI36
NG_008483.1:g.164625C=
NG_008483.2:g.231441C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2577C= MANE Select	ENSP00000356370.3:p.Asn859=
ENST00000638467.1:c.2577C=	ENSP00000491102.1:p.Asn859=
ENST00000681519.1:c.1458C=	ENSP00000505267.1:p.Asn486=
ENST00000367397.1:c.720C=	ENSP00000356367.1:p.Asn240=
ENST00000367399.6:c.2241C=	ENSP00000356369.2:p.Asn747=
ENST00000367400.7:c.2577C=	ENSP00000356370.3:p.Asn859=
ENST00000484075.5:c.2577C=	ENSP00000433932.1:p.Asn859=
ENST00000535699.5:c.2370C=	ENSP00000438786.1:p.Asn790=
ENST00000538660.5:c.2128+5946C=	ENSP00000438091.1:n.2128+5946C=
NM_001193640.1:c.2241C=	NP_001180569.1:p.Asn747=
NM_001257965.1:c.2370C=	NP_001244894.1:p.Asn790=
NM_001257966.1:c.2128+5946C=	NP_001244895.1:n.2128+5946C=
NM_201253.2:c.2577C=	NP_957705.1:p.Asn859=
NR_047563.1:n.2578C=
NR_047564.1:n.2786C=
XM_011509365.1:c.2577C=	XP_011507667.1:p.Asn859=
XM_011509366.1:c.2577C=	XP_011507668.1:p.Asn859=
XM_011509367.1:c.2577C=	XP_011507669.1:p.Asn859=
XM_011509368.1:c.1995C=	XP_011507670.1:p.Asn665=
XM_011509369.1:c.1020C=	XP_011507671.1:p.Asn340=
XM_011509365.2:c.2577C=	XP_011507667.1:p.Asn859=
XM_011509369.2:c.1020C=	XP_011507671.1:p.Asn340=
XM_017000851.1:c.1734C=	XP_016856340.1:p.Asn578=
XM_017000852.1:c.2577C=	XP_016856341.1:p.Asn859=
NM_201253.3:c.2577C= MANE Select	NP_957705.1:p.Asn859=
NM_001193640.2:c.2241C=	NP_001180569.1:p.Asn747=
NM_001257965.2:c.2370C=	NP_001244894.1:p.Asn790=
NR_047563.2:n.2530C=
NR_047564.2:n.2738C=
NM_001257966.2:c.2128+5946C=	NP_001244895.1:n.2128+5946C=