Canonical Allele Identifier: CA1218066495

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427935C= , CM000663.2:g.197427935C=	GRCh38
NC_000001.10:g.197397065C= , CM000663.1:g.197397065C=	GRCh37
NC_000001.9:g.195663688C=	NCBI36
NG_008483.1:g.164658C=
NG_008483.2:g.231474C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2610C= MANE Select	ENSP00000356370.3:p.Asn870=
ENST00000638467.1:c.2610C=	ENSP00000491102.1:p.Asn870=
ENST00000681519.1:c.1491C=	ENSP00000505267.1:p.Asn497=
ENST00000367397.1:c.753C=	ENSP00000356367.1:p.Asn251=
ENST00000367399.6:c.2274C=	ENSP00000356369.2:p.Asn758=
ENST00000367400.7:c.2610C=	ENSP00000356370.3:p.Asn870=
ENST00000484075.5:c.2610C=	ENSP00000433932.1:p.Asn870=
ENST00000535699.5:c.2403C=	ENSP00000438786.1:p.Asn801=
ENST00000538660.5:c.2128+5979C=	ENSP00000438091.1:n.2128+5979C=
NM_001193640.1:c.2274C=	NP_001180569.1:p.Asn758=
NM_001257965.1:c.2403C=	NP_001244894.1:p.Asn801=
NM_001257966.1:c.2128+5979C=	NP_001244895.1:n.2128+5979C=
NM_201253.2:c.2610C=	NP_957705.1:p.Asn870=
NR_047563.1:n.2611C=
NR_047564.1:n.2819C=
XM_011509365.1:c.2610C=	XP_011507667.1:p.Asn870=
XM_011509366.1:c.2610C=	XP_011507668.1:p.Asn870=
XM_011509367.1:c.2610C=	XP_011507669.1:p.Asn870=
XM_011509368.1:c.2028C=	XP_011507670.1:p.Asn676=
XM_011509369.1:c.1053C=	XP_011507671.1:p.Asn351=
XM_011509365.2:c.2610C=	XP_011507667.1:p.Asn870=
XM_011509369.2:c.1053C=	XP_011507671.1:p.Asn351=
XM_017000851.1:c.1767C=	XP_016856340.1:p.Asn589=
XM_017000852.1:c.2610C=	XP_016856341.1:p.Asn870=
NM_201253.3:c.2610C= MANE Select	NP_957705.1:p.Asn870=
NM_001193640.2:c.2274C=	NP_001180569.1:p.Asn758=
NM_001257965.2:c.2403C=	NP_001244894.1:p.Asn801=
NR_047563.2:n.2563C=
NR_047564.2:n.2771C=
NM_001257966.2:c.2128+5979C=	NP_001244895.1:n.2128+5979C=