Canonical Allele Identifier: CA1311782

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197356856C>A , CM000663.2:g.197356856C>A	GRCh38
NC_000001.10:g.197325986C>A , CM000663.1:g.197325986C>A	GRCh37
NC_000001.9:g.195592609C>A	NCBI36
NG_008483.1:g.93579C>A
NG_008483.2:g.160395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1014C>A MANE Select	ENSP00000356370.3:p.Ile338=
ENST00000638467.1:c.1014C>A	ENSP00000491102.1:p.Ile338=
ENST00000367399.6:c.678C>A	ENSP00000356369.2:p.Ile226=
ENST00000367400.7:c.1014C>A	ENSP00000356370.3:p.Ile338=
ENST00000475659.1:n.1151C>A
ENST00000484075.5:c.1014C>A	ENSP00000433932.1:p.Ile338=
ENST00000535699.5:c.807C>A	ENSP00000438786.1:p.Ile269=
ENST00000538660.5:c.1014C>A	ENSP00000438091.1:p.Ile338=
NM_001193640.1:c.678C>A	NP_001180569.1:p.Ile226=
NM_001257965.1:c.807C>A	NP_001244894.1:p.Ile269=
NM_001257966.1:c.1014C>A	NP_001244895.1:p.Ile338=
NM_201253.2:c.1014C>A	NP_957705.1:p.Ile338=
NR_047563.1:n.1223C>A
NR_047564.1:n.1223C>A
XM_011509365.1:c.1014C>A	XP_011507667.1:p.Ile338=
XM_011509366.1:c.1014C>A	XP_011507668.1:p.Ile338=
XM_011509367.1:c.1014C>A	XP_011507669.1:p.Ile338=
XM_011509368.1:c.432C>A	XP_011507670.1:p.Ile144=
XM_011509365.2:c.1014C>A	XP_011507667.1:p.Ile338=
XM_017000851.1:c.171C>A	XP_016856340.1:p.Ile57=
XM_017000852.1:c.1014C>A	XP_016856341.1:p.Ile338=
NM_201253.3:c.1014C>A MANE Select	NP_957705.1:p.Ile338=
NM_001193640.2:c.678C>A	NP_001180569.1:p.Ile226=
NM_001257965.2:c.807C>A	NP_001244894.1:p.Ile269=
NR_047563.2:n.1175C>A
NR_047564.2:n.1175C>A
NM_001257966.2:c.1014C>A	NP_001244895.1:p.Ile338=