Canonical Allele Identifier: CA1141581330

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197328835G= , CM000663.2:g.197328835G=	GRCh38
NC_000001.10:g.197297965G= , CM000663.1:g.197297965G=	GRCh37
NC_000001.9:g.195564588G=	NCBI36
NG_008483.1:g.65558G=
NG_008483.2:g.132374G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.484G= MANE Select	ENSP00000356370.3:p.Val162=
ENST00000638467.1:c.484G=	ENSP00000491102.1:p.Val162=
ENST00000367399.6:c.484G=	ENSP00000356369.2:p.Val162=
ENST00000367400.7:c.484G=	ENSP00000356370.3:p.Val162=
ENST00000475659.1:n.621G=
ENST00000484075.5:c.484G=	ENSP00000433932.1:p.Val162=
ENST00000535699.5:c.277G=	ENSP00000438786.1:p.Val93=
ENST00000538660.5:c.484G=	ENSP00000438091.1:p.Val162=
NM_001193640.1:c.484G=	NP_001180569.1:p.Val162=
NM_001257965.1:c.277G=	NP_001244894.1:p.Val93=
NM_001257966.1:c.484G=	NP_001244895.1:p.Val162=
NM_201253.2:c.484G=	NP_957705.1:p.Val162=
NR_047563.1:n.693G=
NR_047564.1:n.693G=
XM_011509365.1:c.484G=	XP_011507667.1:p.Val162=
XM_011509366.1:c.484G=	XP_011507668.1:p.Val162=
XM_011509367.1:c.484G=	XP_011507669.1:p.Val162=
XM_011509368.1:c.71-15446G=	XP_011507670.1:n.71-15446G=
XM_011509365.2:c.484G=	XP_011507667.1:p.Val162=
XM_017000851.1:c.-220G=	XP_016856340.1:n.-220G=
XM_017000852.1:c.484G=	XP_016856341.1:p.Val162=
NM_201253.3:c.484G= MANE Select	NP_957705.1:p.Val162=
NM_001193640.2:c.484G=	NP_001180569.1:p.Val162=
NM_001257965.2:c.277G=	NP_001244894.1:p.Val93=
NR_047563.2:n.645G=
NR_047564.2:n.645G=
NM_001257966.2:c.484G=	NP_001244895.1:p.Val162=