Canonical Allele Identifier: CA422677460

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446811C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477681C>T , CM000663.2:g.197477681C>T	GRCh38
NC_000001.10:g.197446811C>T , CM000663.1:g.197446811C>T	GRCh37
NC_000001.9:g.195713434C>T	NCBI36
NG_008483.1:g.214404C>T
NG_008483.2:g.281220C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4023C>T MANE Select	ENSP00000356370.3:p.Ile1341=
ENST00000367399.6:c.3687C>T	ENSP00000356369.2:p.Ile1229=
ENST00000367400.7:c.4023C>T	ENSP00000356370.3:p.Ile1341=
ENST00000448952.1:c.257C>T	ENSP00000395407.1:n.257C>T
ENST00000484075.5:c.*134C>T	ENSP00000433932.1:n.*134C>T
ENST00000535699.5:c.3951C>T	ENSP00000438786.1:p.Ile1317=
ENST00000538660.5:c.2415C>T	ENSP00000438091.1:p.Ile805=
NM_001193640.1:c.3687C>T	NP_001180569.1:p.Ile1229=
NM_001257965.1:c.3951C>T	NP_001244894.1:p.Ile1317=
NM_001257966.1:c.2415C>T	NP_001244895.1:p.Ile805=
NM_201253.2:c.4023C>T	NP_957705.1:p.Ile1341=
NR_047563.1:n.4024C>T
NR_047564.1:n.4474C>T
XM_011509366.1:c.*128C>T	XP_011507668.1:n.*128C>T
XM_011509367.1:c.*2C>T	XP_011507669.1:n.*2C>T
XM_011509368.1:c.3441C>T	XP_011507670.1:p.Ile1147=
XM_011509369.1:c.2466C>T	XP_011507671.1:p.Ile822=
XM_011509369.2:c.2466C>T	XP_011507671.1:p.Ile822=
XM_017000851.1:c.3180C>T	XP_016856340.1:p.Ile1060=
XM_017000852.1:c.4158C>T	XP_016856341.1:p.Ile1386=
NM_201253.3:c.4023C>T MANE Select	NP_957705.1:p.Ile1341=
NM_001193640.2:c.3687C>T	NP_001180569.1:p.Ile1229=
NM_001257965.2:c.3951C>T	NP_001244894.1:p.Ile1317=
NR_047563.2:n.3976C>T
NR_047564.2:n.4426C>T
NM_001257966.2:c.2415C>T	NP_001244895.1:p.Ile805=