Canonical Allele Identifier: CA1142299971

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435239C= , CM000663.2:g.197435239C=	GRCh38
NC_000001.10:g.197404369C= , CM000663.1:g.197404369C=	GRCh37
NC_000001.9:g.195670992C=	NCBI36
NG_008483.1:g.171962C=
NG_008483.2:g.238778C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.3376C= MANE Select	ENSP00000356370.3:p.Leu1126=
ENST00000638467.1:c.3376C=	ENSP00000491102.1:p.Leu1126=
ENST00000681519.1:c.2257C=	ENSP00000505267.1:p.Leu753=
ENST00000367397.1:c.1519C=	ENSP00000356367.1:p.Leu507=
ENST00000367399.6:c.3040C=	ENSP00000356369.2:p.Leu1014=
ENST00000367400.7:c.3376C=	ENSP00000356370.3:p.Leu1126=
ENST00000484075.5:c.3376C=	ENSP00000433932.1:p.Leu1126=
ENST00000535699.5:c.3304C=	ENSP00000438786.1:p.Leu1102=
ENST00000538660.5:c.2129-361C=	ENSP00000438091.1:n.2129-361C=
NM_001193640.1:c.3040C=	NP_001180569.1:p.Leu1014=
NM_001257965.1:c.3304C=	NP_001244894.1:p.Leu1102=
NM_001257966.1:c.2129-361C=	NP_001244895.1:n.2129-361C=
NM_201253.2:c.3376C=	NP_957705.1:p.Leu1126=
NR_047563.1:n.3377C=
NR_047564.1:n.3585C=
XM_011509365.1:c.3376C=	XP_011507667.1:p.Leu1126=
XM_011509366.1:c.3376C=	XP_011507668.1:p.Leu1126=
XM_011509367.1:c.3376C=	XP_011507669.1:p.Leu1126=
XM_011509368.1:c.2794C=	XP_011507670.1:p.Leu932=
XM_011509369.1:c.1819C=	XP_011507671.1:p.Leu607=
XM_011509365.2:c.3376C=	XP_011507667.1:p.Leu1126=
XM_011509369.2:c.1819C=	XP_011507671.1:p.Leu607=
XM_017000851.1:c.2533C=	XP_016856340.1:p.Leu845=
XM_017000852.1:c.3511C=	XP_016856341.1:p.Leu1171=
NM_201253.3:c.3376C= MANE Select	NP_957705.1:p.Leu1126=
NM_001193640.2:c.3040C=	NP_001180569.1:p.Leu1014=
NM_001257965.2:c.3304C=	NP_001244894.1:p.Leu1102=
NR_047563.2:n.3329C=
NR_047564.2:n.3537C=
NM_001257966.2:c.2129-361C=	NP_001244895.1:n.2129-361C=