Canonical Allele Identifier: CA1218063264

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421761G= , CM000663.2:g.197421761G=	GRCh38
NC_000001.10:g.197390891G= , CM000663.1:g.197390891G=	GRCh37
NC_000001.9:g.195657514G=	NCBI36
NG_008483.1:g.158484G=
NG_008483.2:g.225300G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1933G= MANE Select	ENSP00000356370.3:p.Asp645=
ENST00000638467.1:c.1933G=	ENSP00000491102.1:p.Asp645=
ENST00000681519.1:c.814G=	ENSP00000505267.1:p.Asp272=
ENST00000367397.1:c.76G=	ENSP00000356367.1:p.Asp26=
ENST00000367399.6:c.1597G=	ENSP00000356369.2:p.Asp533=
ENST00000367400.7:c.1933G=	ENSP00000356370.3:p.Asp645=
ENST00000484075.5:c.1933G=	ENSP00000433932.1:p.Asp645=
ENST00000535699.5:c.1726G=	ENSP00000438786.1:p.Asp576=
ENST00000538660.5:c.1933G=	ENSP00000438091.1:p.Asp645=
NM_001193640.1:c.1597G=	NP_001180569.1:p.Asp533=
NM_001257965.1:c.1726G=	NP_001244894.1:p.Asp576=
NM_001257966.1:c.1933G=	NP_001244895.1:p.Asp645=
NM_201253.2:c.1933G=	NP_957705.1:p.Asp645=
NR_047563.1:n.1934G=
NR_047564.1:n.2142G=
XM_011509365.1:c.1933G=	XP_011507667.1:p.Asp645=
XM_011509366.1:c.1933G=	XP_011507668.1:p.Asp645=
XM_011509367.1:c.1933G=	XP_011507669.1:p.Asp645=
XM_011509368.1:c.1351G=	XP_011507670.1:p.Asp451=
XM_011509369.1:c.376G=	XP_011507671.1:p.Asp126=
XM_011509365.2:c.1933G=	XP_011507667.1:p.Asp645=
XM_011509369.2:c.376G=	XP_011507671.1:p.Asp126=
XM_017000851.1:c.1090G=	XP_016856340.1:p.Asp364=
XM_017000852.1:c.1933G=	XP_016856341.1:p.Asp645=
NM_201253.3:c.1933G= MANE Select	NP_957705.1:p.Asp645=
NM_001193640.2:c.1597G=	NP_001180569.1:p.Asp533=
NM_001257965.2:c.1726G=	NP_001244894.1:p.Asp576=
NR_047563.2:n.1886G=
NR_047564.2:n.2094G=
NM_001257966.2:c.1933G=	NP_001244895.1:p.Asp645=