Canonical Allele Identifier: CA1147864130

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434958G= , CM000663.2:g.197434958G=	GRCh38
NC_000001.10:g.197404088G= , CM000663.1:g.197404088G=	GRCh37
NC_000001.9:g.195670711G=	NCBI36
NG_008483.1:g.171681G=
NG_008483.2:g.238497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3095G= MANE Select	ENSP00000356370.3:p.Gly1032=
ENST00000638467.1:c.3095G=	ENSP00000491102.1:p.Gly1032=
ENST00000681519.1:c.1976G=	ENSP00000505267.1:p.Gly659=
ENST00000367397.1:c.1238G=	ENSP00000356367.1:p.Gly413=
ENST00000367399.6:c.2759G=	ENSP00000356369.2:p.Gly920=
ENST00000367400.7:c.3095G=	ENSP00000356370.3:p.Gly1032=
ENST00000484075.5:c.3095G=	ENSP00000433932.1:p.Gly1032=
ENST00000535699.5:c.3023G=	ENSP00000438786.1:p.Gly1008=
ENST00000538660.5:c.2129-642G=	ENSP00000438091.1:n.2129-642G=
NM_001193640.1:c.2759G=	NP_001180569.1:p.Gly920=
NM_001257965.1:c.3023G=	NP_001244894.1:p.Gly1008=
NM_001257966.1:c.2129-642G=	NP_001244895.1:n.2129-642G=
NM_201253.2:c.3095G=	NP_957705.1:p.Gly1032=
NR_047563.1:n.3096G=
NR_047564.1:n.3304G=
XM_011509365.1:c.3095G=	XP_011507667.1:p.Gly1032=
XM_011509366.1:c.3095G=	XP_011507668.1:p.Gly1032=
XM_011509367.1:c.3095G=	XP_011507669.1:p.Gly1032=
XM_011509368.1:c.2513G=	XP_011507670.1:p.Gly838=
XM_011509369.1:c.1538G=	XP_011507671.1:p.Gly513=
XM_011509365.2:c.3095G=	XP_011507667.1:p.Gly1032=
XM_011509369.2:c.1538G=	XP_011507671.1:p.Gly513=
XM_017000851.1:c.2252G=	XP_016856340.1:p.Gly751=
XM_017000852.1:c.3230G=	XP_016856341.1:p.Gly1077=
NM_201253.3:c.3095G= MANE Select	NP_957705.1:p.Gly1032=
NM_001193640.2:c.2759G=	NP_001180569.1:p.Gly920=
NM_001257965.2:c.3023G=	NP_001244894.1:p.Gly1008=
NR_047563.2:n.3048G=
NR_047564.2:n.3256G=
NM_001257966.2:c.2129-642G=	NP_001244895.1:n.2129-642G=