Canonical Allele Identifier: CA1141934419

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434900C= , CM000663.2:g.197434900C=	GRCh38
NC_000001.10:g.197404030C= , CM000663.1:g.197404030C=	GRCh37
NC_000001.9:g.195670653C=	NCBI36
NG_008483.1:g.171623C=
NG_008483.2:g.238439C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3037C= MANE Select	ENSP00000356370.3:p.Gln1013=
ENST00000638467.1:c.3037C=	ENSP00000491102.1:p.Gln1013=
ENST00000681519.1:c.1918C=	ENSP00000505267.1:p.Gln640=
ENST00000367397.1:c.1180C=	ENSP00000356367.1:p.Gln394=
ENST00000367399.6:c.2701C=	ENSP00000356369.2:p.Gln901=
ENST00000367400.7:c.3037C=	ENSP00000356370.3:p.Gln1013=
ENST00000484075.5:c.3037C=	ENSP00000433932.1:p.Gln1013=
ENST00000535699.5:c.2965C=	ENSP00000438786.1:p.Gln989=
ENST00000538660.5:c.2129-700C=	ENSP00000438091.1:n.2129-700C=
NM_001193640.1:c.2701C=	NP_001180569.1:p.Gln901=
NM_001257965.1:c.2965C=	NP_001244894.1:p.Gln989=
NM_001257966.1:c.2129-700C=	NP_001244895.1:n.2129-700C=
NM_201253.2:c.3037C=	NP_957705.1:p.Gln1013=
NR_047563.1:n.3038C=
NR_047564.1:n.3246C=
XM_011509365.1:c.3037C=	XP_011507667.1:p.Gln1013=
XM_011509366.1:c.3037C=	XP_011507668.1:p.Gln1013=
XM_011509367.1:c.3037C=	XP_011507669.1:p.Gln1013=
XM_011509368.1:c.2455C=	XP_011507670.1:p.Gln819=
XM_011509369.1:c.1480C=	XP_011507671.1:p.Gln494=
XM_011509365.2:c.3037C=	XP_011507667.1:p.Gln1013=
XM_011509369.2:c.1480C=	XP_011507671.1:p.Gln494=
XM_017000851.1:c.2194C=	XP_016856340.1:p.Gln732=
XM_017000852.1:c.3172C=	XP_016856341.1:p.Gln1058=
NM_201253.3:c.3037C= MANE Select	NP_957705.1:p.Gln1013=
NM_001193640.2:c.2701C=	NP_001180569.1:p.Gln901=
NM_001257965.2:c.2965C=	NP_001244894.1:p.Gln989=
NR_047563.2:n.2990C=
NR_047564.2:n.3198C=
NM_001257966.2:c.2129-700C=	NP_001244895.1:n.2129-700C=