Canonical Allele Identifier: CA1218068735

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434961C= , CM000663.2:g.197434961C=	GRCh38
NC_000001.10:g.197404091C= , CM000663.1:g.197404091C=	GRCh37
NC_000001.9:g.195670714C=	NCBI36
NG_008483.1:g.171684C=
NG_008483.2:g.238500C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3098C= MANE Select	ENSP00000356370.3:p.Thr1033=
ENST00000638467.1:c.3098C=	ENSP00000491102.1:p.Thr1033=
ENST00000681519.1:c.1979C=	ENSP00000505267.1:p.Thr660=
ENST00000367397.1:c.1241C=	ENSP00000356367.1:p.Thr414=
ENST00000367399.6:c.2762C=	ENSP00000356369.2:p.Thr921=
ENST00000367400.7:c.3098C=	ENSP00000356370.3:p.Thr1033=
ENST00000484075.5:c.3098C=	ENSP00000433932.1:p.Thr1033=
ENST00000535699.5:c.3026C=	ENSP00000438786.1:p.Thr1009=
ENST00000538660.5:c.2129-639C=	ENSP00000438091.1:n.2129-639C=
NM_001193640.1:c.2762C=	NP_001180569.1:p.Thr921=
NM_001257965.1:c.3026C=	NP_001244894.1:p.Thr1009=
NM_001257966.1:c.2129-639C=	NP_001244895.1:n.2129-639C=
NM_201253.2:c.3098C=	NP_957705.1:p.Thr1033=
NR_047563.1:n.3099C=
NR_047564.1:n.3307C=
XM_011509365.1:c.3098C=	XP_011507667.1:p.Thr1033=
XM_011509366.1:c.3098C=	XP_011507668.1:p.Thr1033=
XM_011509367.1:c.3098C=	XP_011507669.1:p.Thr1033=
XM_011509368.1:c.2516C=	XP_011507670.1:p.Thr839=
XM_011509369.1:c.1541C=	XP_011507671.1:p.Thr514=
XM_011509365.2:c.3098C=	XP_011507667.1:p.Thr1033=
XM_011509369.2:c.1541C=	XP_011507671.1:p.Thr514=
XM_017000851.1:c.2255C=	XP_016856340.1:p.Thr752=
XM_017000852.1:c.3233C=	XP_016856341.1:p.Thr1078=
NM_201253.3:c.3098C= MANE Select	NP_957705.1:p.Thr1033=
NM_001193640.2:c.2762C=	NP_001180569.1:p.Thr921=
NM_001257965.2:c.3026C=	NP_001244894.1:p.Thr1009=
NR_047563.2:n.3051C=
NR_047564.2:n.3259C=
NM_001257966.2:c.2129-639C=	NP_001244895.1:n.2129-639C=