Canonical Allele Identifier: CA1218062994

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421070C= , CM000663.2:g.197421070C=	GRCh38
NC_000001.10:g.197390200C= , CM000663.1:g.197390200C=	GRCh37
NC_000001.9:g.195656823C=	NCBI36
NG_008483.1:g.157793C=
NG_008483.2:g.224609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1242C= MANE Select	ENSP00000356370.3:p.Asn414=
ENST00000638467.1:c.1242C=	ENSP00000491102.1:p.Asn414=
ENST00000681519.1:c.123C=	ENSP00000505267.1:p.Asn41=
ENST00000367397.1:c.-616C=	ENSP00000356367.1:n.-616C=
ENST00000367399.6:c.906C=	ENSP00000356369.2:p.Asn302=
ENST00000367400.7:c.1242C=	ENSP00000356370.3:p.Asn414=
ENST00000476483.1:n.202C=
ENST00000484075.5:c.1242C=	ENSP00000433932.1:p.Asn414=
ENST00000535699.5:c.1035C=	ENSP00000438786.1:p.Asn345=
ENST00000538660.5:c.1242C=	ENSP00000438091.1:p.Asn414=
NM_001193640.1:c.906C=	NP_001180569.1:p.Asn302=
NM_001257965.1:c.1035C=	NP_001244894.1:p.Asn345=
NM_001257966.1:c.1242C=	NP_001244895.1:p.Asn414=
NM_201253.2:c.1242C=	NP_957705.1:p.Asn414=
NR_047563.1:n.1451C=
NR_047564.1:n.1451C=
XM_011509365.1:c.1242C=	XP_011507667.1:p.Asn414=
XM_011509366.1:c.1242C=	XP_011507668.1:p.Asn414=
XM_011509367.1:c.1242C=	XP_011507669.1:p.Asn414=
XM_011509368.1:c.660C=	XP_011507670.1:p.Asn220=
XM_011509369.1:c.-316C=	XP_011507671.1:n.-316C=
XM_011509365.2:c.1242C=	XP_011507667.1:p.Asn414=
XM_011509369.2:c.-316C=	XP_011507671.1:n.-316C=
XM_017000851.1:c.399C=	XP_016856340.1:p.Asn133=
XM_017000852.1:c.1242C=	XP_016856341.1:p.Asn414=
NM_201253.3:c.1242C= MANE Select	NP_957705.1:p.Asn414=
NM_001193640.2:c.906C=	NP_001180569.1:p.Asn302=
NM_001257965.2:c.1035C=	NP_001244894.1:p.Asn345=
NR_047563.2:n.1403C=
NR_047564.2:n.1403C=
NM_001257966.2:c.1242C=	NP_001244895.1:p.Asn414=