Canonical Allele Identifier: CA1218068677

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434814A= , CM000663.2:g.197434814A=	GRCh38
NC_000001.10:g.197403944A= , CM000663.1:g.197403944A=	GRCh37
NC_000001.9:g.195670567A=	NCBI36
NG_008483.1:g.171537A=
NG_008483.2:g.238353A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2951A= MANE Select	ENSP00000356370.3:p.Asp984=
ENST00000638467.1:c.2951A=	ENSP00000491102.1:p.Asp984=
ENST00000681519.1:c.1832A=	ENSP00000505267.1:p.Asp611=
ENST00000367397.1:c.1094A=	ENSP00000356367.1:p.Asp365=
ENST00000367399.6:c.2615A=	ENSP00000356369.2:p.Asp872=
ENST00000367400.7:c.2951A=	ENSP00000356370.3:p.Asp984=
ENST00000484075.5:c.2951A=	ENSP00000433932.1:p.Asp984=
ENST00000535699.5:c.2879A=	ENSP00000438786.1:p.Asp960=
ENST00000538660.5:c.2129-786A=	ENSP00000438091.1:n.2129-786A=
NM_001193640.1:c.2615A=	NP_001180569.1:p.Asp872=
NM_001257965.1:c.2879A=	NP_001244894.1:p.Asp960=
NM_001257966.1:c.2129-786A=	NP_001244895.1:n.2129-786A=
NM_201253.2:c.2951A=	NP_957705.1:p.Asp984=
NR_047563.1:n.2952A=
NR_047564.1:n.3160A=
XM_011509365.1:c.2951A=	XP_011507667.1:p.Asp984=
XM_011509366.1:c.2951A=	XP_011507668.1:p.Asp984=
XM_011509367.1:c.2951A=	XP_011507669.1:p.Asp984=
XM_011509368.1:c.2369A=	XP_011507670.1:p.Asp790=
XM_011509369.1:c.1394A=	XP_011507671.1:p.Asp465=
XM_011509365.2:c.2951A=	XP_011507667.1:p.Asp984=
XM_011509369.2:c.1394A=	XP_011507671.1:p.Asp465=
XM_017000851.1:c.2108A=	XP_016856340.1:p.Asp703=
XM_017000852.1:c.3086A=	XP_016856341.1:p.Asp1029=
NM_201253.3:c.2951A= MANE Select	NP_957705.1:p.Asp984=
NM_001193640.2:c.2615A=	NP_001180569.1:p.Asp872=
NM_001257965.2:c.2879A=	NP_001244894.1:p.Asp960=
NR_047563.2:n.2904A=
NR_047564.2:n.3112A=
NM_001257966.2:c.2129-786A=	NP_001244895.1:n.2129-786A=