Canonical Allele Identifier: CA1218063204

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421611G= , CM000663.2:g.197421611G=	GRCh38
NC_000001.10:g.197390741G= , CM000663.1:g.197390741G=	GRCh37
NC_000001.9:g.195657364G=	NCBI36
NG_008483.1:g.158334G=
NG_008483.2:g.225150G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1783G= MANE Select	ENSP00000356370.3:p.Ala595=
ENST00000638467.1:c.1783G=	ENSP00000491102.1:p.Ala595=
ENST00000681519.1:c.664G=	ENSP00000505267.1:p.Ala222=
ENST00000367397.1:c.-75G=	ENSP00000356367.1:n.-75G=
ENST00000367399.6:c.1447G=	ENSP00000356369.2:p.Ala483=
ENST00000367400.7:c.1783G=	ENSP00000356370.3:p.Ala595=
ENST00000484075.5:c.1783G=	ENSP00000433932.1:p.Ala595=
ENST00000535699.5:c.1576G=	ENSP00000438786.1:p.Ala526=
ENST00000538660.5:c.1783G=	ENSP00000438091.1:p.Ala595=
NM_001193640.1:c.1447G=	NP_001180569.1:p.Ala483=
NM_001257965.1:c.1576G=	NP_001244894.1:p.Ala526=
NM_001257966.1:c.1783G=	NP_001244895.1:p.Ala595=
NM_201253.2:c.1783G=	NP_957705.1:p.Ala595=
NR_047563.1:n.1922+70G=
NR_047564.1:n.1992G=
XM_011509365.1:c.1783G=	XP_011507667.1:p.Ala595=
XM_011509366.1:c.1783G=	XP_011507668.1:p.Ala595=
XM_011509367.1:c.1783G=	XP_011507669.1:p.Ala595=
XM_011509368.1:c.1201G=	XP_011507670.1:p.Ala401=
XM_011509369.1:c.226G=	XP_011507671.1:p.Ala76=
XM_011509365.2:c.1783G=	XP_011507667.1:p.Ala595=
XM_011509369.2:c.226G=	XP_011507671.1:p.Ala76=
XM_017000851.1:c.940G=	XP_016856340.1:p.Ala314=
XM_017000852.1:c.1783G=	XP_016856341.1:p.Ala595=
NM_201253.3:c.1783G= MANE Select	NP_957705.1:p.Ala595=
NM_001193640.2:c.1447G=	NP_001180569.1:p.Ala483=
NM_001257965.2:c.1576G=	NP_001244894.1:p.Ala526=
NR_047563.2:n.1874+70G=
NR_047564.2:n.1944G=
NM_001257966.2:c.1783G=	NP_001244895.1:p.Ala595=