Canonical Allele Identifier: CA422677441

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446799A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477669A>T , CM000663.2:g.197477669A>T	GRCh38
NC_000001.10:g.197446799A>T , CM000663.1:g.197446799A>T	GRCh37
NC_000001.9:g.195713422A>T	NCBI36
NG_008483.1:g.214392A>T
NG_008483.2:g.281208A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4011A>T MANE Select	ENSP00000356370.3:p.Ala1337=
ENST00000367399.6:c.3675A>T	ENSP00000356369.2:p.Ala1225=
ENST00000367400.7:c.4011A>T	ENSP00000356370.3:p.Ala1337=
ENST00000448952.1:c.245A>T	ENSP00000395407.1:n.245A>T
ENST00000484075.5:c.*122A>T	ENSP00000433932.1:n.*122A>T
ENST00000535699.5:c.3939A>T	ENSP00000438786.1:p.Ala1313=
ENST00000538660.5:c.2403A>T	ENSP00000438091.1:p.Ala801=
NM_001193640.1:c.3675A>T	NP_001180569.1:p.Ala1225=
NM_001257965.1:c.3939A>T	NP_001244894.1:p.Ala1313=
NM_001257966.1:c.2403A>T	NP_001244895.1:p.Ala801=
NM_201253.2:c.4011A>T	NP_957705.1:p.Ala1337=
NR_047563.1:n.4012A>T
NR_047564.1:n.4462A>T
XM_011509366.1:c.*116A>T	XP_011507668.1:n.*116A>T
XM_011509367.1:c.3884A>T	XP_011507669.1:p.Gln1295Leu
XM_011509368.1:c.3429A>T	XP_011507670.1:p.Ala1143=
XM_011509369.1:c.2454A>T	XP_011507671.1:p.Ala818=
XM_011509369.2:c.2454A>T	XP_011507671.1:p.Ala818=
XM_017000851.1:c.3168A>T	XP_016856340.1:p.Ala1056=
XM_017000852.1:c.4146A>T	XP_016856341.1:p.Ala1382=
NM_201253.3:c.4011A>T MANE Select	NP_957705.1:p.Ala1337=
NM_001193640.2:c.3675A>T	NP_001180569.1:p.Ala1225=
NM_001257965.2:c.3939A>T	NP_001244894.1:p.Ala1313=
NR_047563.2:n.3964A>T
NR_047564.2:n.4414A>T
NM_001257966.2:c.2403A>T	NP_001244895.1:p.Ala801=