Canonical Allele Identifier: CA1218066134

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427652C= , CM000663.2:g.197427652C=	GRCh38
NC_000001.10:g.197396782C= , CM000663.1:g.197396782C=	GRCh37
NC_000001.9:g.195663405C=	NCBI36
NG_008483.1:g.164375C=
NG_008483.2:g.231191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2327C= MANE Select	ENSP00000356370.3:p.Thr776=
ENST00000638467.1:c.2327C=	ENSP00000491102.1:p.Thr776=
ENST00000681519.1:c.1208C=	ENSP00000505267.1:p.Thr403=
ENST00000367397.1:c.470C=	ENSP00000356367.1:p.Thr157=
ENST00000367399.6:c.1991C=	ENSP00000356369.2:p.Thr664=
ENST00000367400.7:c.2327C=	ENSP00000356370.3:p.Thr776=
ENST00000480086.2:n.228C=
ENST00000484075.5:c.2327C=	ENSP00000433932.1:p.Thr776=
ENST00000535699.5:c.2120C=	ENSP00000438786.1:p.Thr707=
ENST00000538660.5:c.2128+5696C=	ENSP00000438091.1:n.2128+5696C=
NM_001193640.1:c.1991C=	NP_001180569.1:p.Thr664=
NM_001257965.1:c.2120C=	NP_001244894.1:p.Thr707=
NM_001257966.1:c.2128+5696C=	NP_001244895.1:n.2128+5696C=
NM_201253.2:c.2327C=	NP_957705.1:p.Thr776=
NR_047563.1:n.2328C=
NR_047564.1:n.2536C=
XM_011509365.1:c.2327C=	XP_011507667.1:p.Thr776=
XM_011509366.1:c.2327C=	XP_011507668.1:p.Thr776=
XM_011509367.1:c.2327C=	XP_011507669.1:p.Thr776=
XM_011509368.1:c.1745C=	XP_011507670.1:p.Thr582=
XM_011509369.1:c.770C=	XP_011507671.1:p.Thr257=
XM_011509365.2:c.2327C=	XP_011507667.1:p.Thr776=
XM_011509369.2:c.770C=	XP_011507671.1:p.Thr257=
XM_017000851.1:c.1484C=	XP_016856340.1:p.Thr495=
XM_017000852.1:c.2327C=	XP_016856341.1:p.Thr776=
NM_201253.3:c.2327C= MANE Select	NP_957705.1:p.Thr776=
NM_001193640.2:c.1991C=	NP_001180569.1:p.Thr664=
NM_001257965.2:c.2120C=	NP_001244894.1:p.Thr707=
NR_047563.2:n.2280C=
NR_047564.2:n.2488C=
NM_001257966.2:c.2128+5696C=	NP_001244895.1:n.2128+5696C=