Canonical Allele Identifier: CA344035946

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446968T>A (hg19) ; chr1:g.197477838T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477838T>A , CM000663.2:g.197477838T>A	GRCh38
NC_000001.10:g.197446968T>A , CM000663.1:g.197446968T>A	GRCh37
NC_000001.9:g.195713591T>A	NCBI36
NG_008483.1:g.214561T>A
NG_008483.2:g.281377T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4180T>A MANE Select	ENSP00000356370.3:p.Trp1394Arg
ENST00000367399.6:c.3844T>A	ENSP00000356369.2:p.Trp1282Arg
ENST00000367400.7:c.4180T>A	ENSP00000356370.3:p.Trp1394Arg
ENST00000448952.1:c.414T>A	ENSP00000395407.1:n.414T>A
ENST00000484075.5:c.*291T>A	ENSP00000433932.1:n.*291T>A
ENST00000535699.5:c.4108T>A	ENSP00000438786.1:p.Trp1370Arg
ENST00000538660.5:c.2572T>A	ENSP00000438091.1:p.Trp858Arg
NM_001193640.1:c.3844T>A	NP_001180569.1:p.Trp1282Arg
NM_001257965.1:c.4108T>A	NP_001244894.1:p.Trp1370Arg
NM_001257966.1:c.2572T>A	NP_001244895.1:p.Trp858Arg
NM_201253.2:c.4180T>A	NP_957705.1:p.Trp1394Arg
NR_047563.1:n.4181T>A
NR_047564.1:n.4631T>A
XM_011509366.1:c.*285T>A	XP_011507668.1:n.*285T>A
XM_011509367.1:c.*159T>A	XP_011507669.1:n.*159T>A
XM_011509368.1:c.3598T>A	XP_011507670.1:p.Trp1200Arg
XM_011509369.1:c.2623T>A	XP_011507671.1:p.Trp875Arg
XM_011509369.2:c.2623T>A	XP_011507671.1:p.Trp875Arg
XM_017000851.1:c.3337T>A	XP_016856340.1:p.Trp1113Arg
XM_017000852.1:c.4315T>A	XP_016856341.1:p.Trp1439Arg
NM_201253.3:c.4180T>A MANE Select	NP_957705.1:p.Trp1394Arg
NM_001193640.2:c.3844T>A	NP_001180569.1:p.Trp1282Arg
NM_001257965.2:c.4108T>A	NP_001244894.1:p.Trp1370Arg
NR_047563.2:n.4133T>A
NR_047564.2:n.4583T>A
NM_001257966.2:c.2572T>A	NP_001244895.1:p.Trp858Arg