Canonical Allele Identifier: CA1218068694

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434855T= , CM000663.2:g.197434855T=	GRCh38
NC_000001.10:g.197403985T= , CM000663.1:g.197403985T=	GRCh37
NC_000001.9:g.195670608T=	NCBI36
NG_008483.1:g.171578T=
NG_008483.2:g.238394T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2992T= MANE Select	ENSP00000356370.3:p.Phe998=
ENST00000638467.1:c.2992T=	ENSP00000491102.1:p.Phe998=
ENST00000681519.1:c.1873T=	ENSP00000505267.1:p.Phe625=
ENST00000367397.1:c.1135T=	ENSP00000356367.1:p.Phe379=
ENST00000367399.6:c.2656T=	ENSP00000356369.2:p.Phe886=
ENST00000367400.7:c.2992T=	ENSP00000356370.3:p.Phe998=
ENST00000484075.5:c.2992T=	ENSP00000433932.1:p.Phe998=
ENST00000535699.5:c.2920T=	ENSP00000438786.1:p.Phe974=
ENST00000538660.5:c.2129-745T=	ENSP00000438091.1:n.2129-745T=
NM_001193640.1:c.2656T=	NP_001180569.1:p.Phe886=
NM_001257965.1:c.2920T=	NP_001244894.1:p.Phe974=
NM_001257966.1:c.2129-745T=	NP_001244895.1:n.2129-745T=
NM_201253.2:c.2992T=	NP_957705.1:p.Phe998=
NR_047563.1:n.2993T=
NR_047564.1:n.3201T=
XM_011509365.1:c.2992T=	XP_011507667.1:p.Phe998=
XM_011509366.1:c.2992T=	XP_011507668.1:p.Phe998=
XM_011509367.1:c.2992T=	XP_011507669.1:p.Phe998=
XM_011509368.1:c.2410T=	XP_011507670.1:p.Phe804=
XM_011509369.1:c.1435T=	XP_011507671.1:p.Phe479=
XM_011509365.2:c.2992T=	XP_011507667.1:p.Phe998=
XM_011509369.2:c.1435T=	XP_011507671.1:p.Phe479=
XM_017000851.1:c.2149T=	XP_016856340.1:p.Phe717=
XM_017000852.1:c.3127T=	XP_016856341.1:p.Phe1043=
NM_201253.3:c.2992T= MANE Select	NP_957705.1:p.Phe998=
NM_001193640.2:c.2656T=	NP_001180569.1:p.Phe886=
NM_001257965.2:c.2920T=	NP_001244894.1:p.Phe974=
NR_047563.2:n.2945T=
NR_047564.2:n.3153T=
NM_001257966.2:c.2129-745T=	NP_001244895.1:n.2129-745T=