Canonical Allele Identifier: CA1218065659

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429534C= , CM000663.2:g.197429534C=	GRCh38
NC_000001.10:g.197398664C= , CM000663.1:g.197398664C=	GRCh37
NC_000001.9:g.195665287C=	NCBI36
NG_008483.1:g.166257C=
NG_008483.2:g.233073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2762C= MANE Select	ENSP00000356370.3:p.Ala921=
ENST00000638467.1:c.2762C=	ENSP00000491102.1:p.Ala921=
ENST00000681519.1:c.1643C=	ENSP00000505267.1:p.Ala548=
ENST00000367397.1:c.905C=	ENSP00000356367.1:p.Ala302=
ENST00000367399.6:c.2426C=	ENSP00000356369.2:p.Ala809=
ENST00000367400.7:c.2762C=	ENSP00000356370.3:p.Ala921=
ENST00000484075.5:c.2762C=	ENSP00000433932.1:p.Ala921=
ENST00000535699.5:c.2690C=	ENSP00000438786.1:p.Ala897=
ENST00000538660.5:c.2129-6066C=	ENSP00000438091.1:n.2129-6066C=
NM_001193640.1:c.2426C=	NP_001180569.1:p.Ala809=
NM_001257965.1:c.2690C=	NP_001244894.1:p.Ala897=
NM_001257966.1:c.2129-6066C=	NP_001244895.1:n.2129-6066C=
NM_201253.2:c.2762C=	NP_957705.1:p.Ala921=
NR_047563.1:n.2763C=
NR_047564.1:n.2971C=
XM_011509365.1:c.2762C=	XP_011507667.1:p.Ala921=
XM_011509366.1:c.2762C=	XP_011507668.1:p.Ala921=
XM_011509367.1:c.2762C=	XP_011507669.1:p.Ala921=
XM_011509368.1:c.2180C=	XP_011507670.1:p.Ala727=
XM_011509369.1:c.1205C=	XP_011507671.1:p.Ala402=
XM_011509365.2:c.2762C=	XP_011507667.1:p.Ala921=
XM_011509369.2:c.1205C=	XP_011507671.1:p.Ala402=
XM_017000851.1:c.1919C=	XP_016856340.1:p.Ala640=
XM_017000852.1:c.2897C=	XP_016856341.1:p.Ala966=
NM_201253.3:c.2762C= MANE Select	NP_957705.1:p.Ala921=
NM_001193640.2:c.2426C=	NP_001180569.1:p.Ala809=
NM_001257965.2:c.2690C=	NP_001244894.1:p.Ala897=
NR_047563.2:n.2715C=
NR_047564.2:n.2923C=
NM_001257966.2:c.2129-6066C=	NP_001244895.1:n.2129-6066C=