Canonical Allele Identifier: CA1218068612

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434637T= , CM000663.2:g.197434637T=	GRCh38
NC_000001.10:g.197403767T= , CM000663.1:g.197403767T=	GRCh37
NC_000001.9:g.195670390T=	NCBI36
NG_008483.1:g.171360T=
NG_008483.2:g.238176T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.2843-69T= MANE Select	ENSP00000356370.3:n.2843-69T=
ENST00000638467.1:c.2843-69T=	ENSP00000491102.1:n.2843-69T=
ENST00000681519.1:c.1724-69T=	ENSP00000505267.1:n.1724-69T=
ENST00000367397.1:c.986-69T=	ENSP00000356367.1:n.986-69T=
ENST00000367399.6:c.2507-69T=	ENSP00000356369.2:n.2507-69T=
ENST00000367400.7:c.2843-69T=	ENSP00000356370.3:n.2843-69T=
ENST00000484075.5:c.2843-69T=	ENSP00000433932.1:n.2843-69T=
ENST00000535699.5:c.2771-69T=	ENSP00000438786.1:n.2771-69T=
ENST00000538660.5:c.2129-963T=	ENSP00000438091.1:n.2129-963T=
NM_001193640.1:c.2507-69T=	NP_001180569.1:n.2507-69T=
NM_001257965.1:c.2771-69T=	NP_001244894.1:n.2771-69T=
NM_001257966.1:c.2129-963T=	NP_001244895.1:n.2129-963T=
NM_201253.2:c.2843-69T=	NP_957705.1:n.2843-69T=
NR_047563.1:n.2844-69T=
NR_047564.1:n.3052-69T=
XM_011509365.1:c.2843-69T=	XP_011507667.1:n.2843-69T=
XM_011509366.1:c.2843-69T=	XP_011507668.1:n.2843-69T=
XM_011509367.1:c.2843-69T=	XP_011507669.1:n.2843-69T=
XM_011509368.1:c.2261-69T=	XP_011507670.1:n.2261-69T=
XM_011509369.1:c.1286-69T=	XP_011507671.1:n.1286-69T=
XM_011509365.2:c.2843-69T=	XP_011507667.1:n.2843-69T=
XM_011509369.2:c.1286-69T=	XP_011507671.1:n.1286-69T=
XM_017000851.1:c.2000-69T=	XP_016856340.1:n.2000-69T=
XM_017000852.1:c.2978-69T=	XP_016856341.1:n.2978-69T=
NM_201253.3:c.2843-69T= MANE Select	NP_957705.1:n.2843-69T=
NM_001193640.2:c.2507-69T=	NP_001180569.1:n.2507-69T=
NM_001257965.2:c.2771-69T=	NP_001244894.1:n.2771-69T=
NR_047563.2:n.2796-69T=
NR_047564.2:n.3004-69T=
NM_001257966.2:c.2129-963T=	NP_001244895.1:n.2129-963T=