Canonical Allele Identifier: CA1218063008

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421109C= , CM000663.2:g.197421109C=	GRCh38
NC_000001.10:g.197390239C= , CM000663.1:g.197390239C=	GRCh37
NC_000001.9:g.195656862C=	NCBI36
NG_008483.1:g.157832C=
NG_008483.2:g.224648C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1281C= MANE Select	ENSP00000356370.3:p.Asn427=
ENST00000638467.1:c.1281C=	ENSP00000491102.1:p.Asn427=
ENST00000681519.1:c.162C=	ENSP00000505267.1:p.Asn54=
ENST00000367397.1:c.-577C=	ENSP00000356367.1:n.-577C=
ENST00000367399.6:c.945C=	ENSP00000356369.2:p.Asn315=
ENST00000367400.7:c.1281C=	ENSP00000356370.3:p.Asn427=
ENST00000476483.1:n.241C=
ENST00000484075.5:c.1281C=	ENSP00000433932.1:p.Asn427=
ENST00000535699.5:c.1074C=	ENSP00000438786.1:p.Asn358=
ENST00000538660.5:c.1281C=	ENSP00000438091.1:p.Asn427=
NM_001193640.1:c.945C=	NP_001180569.1:p.Asn315=
NM_001257965.1:c.1074C=	NP_001244894.1:p.Asn358=
NM_001257966.1:c.1281C=	NP_001244895.1:p.Asn427=
NM_201253.2:c.1281C=	NP_957705.1:p.Asn427=
NR_047563.1:n.1490C=
NR_047564.1:n.1490C=
XM_011509365.1:c.1281C=	XP_011507667.1:p.Asn427=
XM_011509366.1:c.1281C=	XP_011507668.1:p.Asn427=
XM_011509367.1:c.1281C=	XP_011507669.1:p.Asn427=
XM_011509368.1:c.699C=	XP_011507670.1:p.Asn233=
XM_011509369.1:c.-277C=	XP_011507671.1:n.-277C=
XM_011509365.2:c.1281C=	XP_011507667.1:p.Asn427=
XM_011509369.2:c.-277C=	XP_011507671.1:n.-277C=
XM_017000851.1:c.438C=	XP_016856340.1:p.Asn146=
XM_017000852.1:c.1281C=	XP_016856341.1:p.Asn427=
NM_201253.3:c.1281C= MANE Select	NP_957705.1:p.Asn427=
NM_001193640.2:c.945C=	NP_001180569.1:p.Asn315=
NM_001257965.2:c.1074C=	NP_001244894.1:p.Asn358=
NR_047563.2:n.1442C=
NR_047564.2:n.1442C=
NM_001257966.2:c.1281C=	NP_001244895.1:p.Asn427=