Canonical Allele Identifier: CA1149143994

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427716T= , CM000663.2:g.197427716T=	GRCh38
NC_000001.10:g.197396846T= , CM000663.1:g.197396846T=	GRCh37
NC_000001.9:g.195663469T=	NCBI36
NG_008483.1:g.164439T=
NG_008483.2:g.231255T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2391T= MANE Select	ENSP00000356370.3:p.Ser797=
ENST00000638467.1:c.2391T=	ENSP00000491102.1:p.Ser797=
ENST00000681519.1:c.1272T=	ENSP00000505267.1:p.Ser424=
ENST00000367397.1:c.534T=	ENSP00000356367.1:p.Ser178=
ENST00000367399.6:c.2055T=	ENSP00000356369.2:p.Ser685=
ENST00000367400.7:c.2391T=	ENSP00000356370.3:p.Ser797=
ENST00000480086.2:n.292T=
ENST00000484075.5:c.2391T=	ENSP00000433932.1:p.Ser797=
ENST00000535699.5:c.2184T=	ENSP00000438786.1:p.Ser728=
ENST00000538660.5:c.2128+5760T=	ENSP00000438091.1:n.2128+5760T=
NM_001193640.1:c.2055T=	NP_001180569.1:p.Ser685=
NM_001257965.1:c.2184T=	NP_001244894.1:p.Ser728=
NM_001257966.1:c.2128+5760T=	NP_001244895.1:n.2128+5760T=
NM_201253.2:c.2391T=	NP_957705.1:p.Ser797=
NR_047563.1:n.2392T=
NR_047564.1:n.2600T=
XM_011509365.1:c.2391T=	XP_011507667.1:p.Ser797=
XM_011509366.1:c.2391T=	XP_011507668.1:p.Ser797=
XM_011509367.1:c.2391T=	XP_011507669.1:p.Ser797=
XM_011509368.1:c.1809T=	XP_011507670.1:p.Ser603=
XM_011509369.1:c.834T=	XP_011507671.1:p.Ser278=
XM_011509365.2:c.2391T=	XP_011507667.1:p.Ser797=
XM_011509369.2:c.834T=	XP_011507671.1:p.Ser278=
XM_017000851.1:c.1548T=	XP_016856340.1:p.Ser516=
XM_017000852.1:c.2391T=	XP_016856341.1:p.Ser797=
NM_201253.3:c.2391T= MANE Select	NP_957705.1:p.Ser797=
NM_001193640.2:c.2055T=	NP_001180569.1:p.Ser685=
NM_001257965.2:c.2184T=	NP_001244894.1:p.Ser728=
NR_047563.2:n.2344T=
NR_047564.2:n.2552T=
NM_001257966.2:c.2128+5760T=	NP_001244895.1:n.2128+5760T=