Canonical Allele Identifier: CA1145005953

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197478078A= , CM000663.2:g.197478078A=	GRCh38
NC_000001.10:g.197447208A= , CM000663.1:g.197447208A=	GRCh37
NC_000001.9:g.195713831A=	NCBI36
NG_008483.1:g.214801A=
NG_008483.2:g.281617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.*199A= MANE Select	ENSP00000356370.3:n.*199A=
ENST00000367400.7:c.*199A=	ENSP00000356370.3:n.*199A=
ENST00000448952.1:c.654A=	ENSP00000395407.1:n.654A=
ENST00000484075.5:c.*531A=	ENSP00000433932.1:n.*531A=
ENST00000535699.5:c.*199A=	ENSP00000438786.1:n.*199A=
ENST00000538660.5:c.*199A=	ENSP00000438091.1:n.*199A=
NM_001193640.1:c.*199A=	NP_001180569.1:n.*199A=
NM_001257965.1:c.*199A=	NP_001244894.1:n.*199A=
NM_001257966.1:c.*199A=	NP_001244895.1:n.*199A=
NM_201253.2:c.*199A=	NP_957705.1:n.*199A=
NR_047563.1:n.4421A=
NR_047564.1:n.4871A=
XM_011509366.1:c.*525A=	XP_011507668.1:n.*525A=
XM_011509367.1:c.*399A=	XP_011507669.1:n.*399A=
XM_011509368.1:c.*199A=	XP_011507670.1:n.*199A=
XM_011509369.1:c.*199A=	XP_011507671.1:n.*199A=
XM_011509369.2:c.*199A=	XP_011507671.1:n.*199A=
XM_017000851.1:c.*199A=	XP_016856340.1:n.*199A=
XM_017000852.1:c.*199A=	XP_016856341.1:n.*199A=
NM_201253.3:c.*199A= MANE Select	NP_957705.1:n.*199A=
NM_001193640.2:c.*199A=	NP_001180569.1:n.*199A=
NM_001257965.2:c.*199A=	NP_001244894.1:n.*199A=
NR_047563.2:n.4373A=
NR_047564.2:n.4823A=
NM_001257966.2:c.*199A=	NP_001244895.1:n.*199A=