Canonical Allele Identifier: CA344035958

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446970G>T (hg19) ; chr1:g.197477840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477840G>T , CM000663.2:g.197477840G>T	GRCh38
NC_000001.10:g.197446970G>T , CM000663.1:g.197446970G>T	GRCh37
NC_000001.9:g.195713593G>T	NCBI36
NG_008483.1:g.214563G>T
NG_008483.2:g.281379G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4182G>T MANE Select	ENSP00000356370.3:p.Trp1394Cys
ENST00000367399.6:c.3846G>T	ENSP00000356369.2:p.Trp1282Cys
ENST00000367400.7:c.4182G>T	ENSP00000356370.3:p.Trp1394Cys
ENST00000448952.1:c.416G>T	ENSP00000395407.1:n.416G>T
ENST00000484075.5:c.*293G>T	ENSP00000433932.1:n.*293G>T
ENST00000535699.5:c.4110G>T	ENSP00000438786.1:p.Trp1370Cys
ENST00000538660.5:c.2574G>T	ENSP00000438091.1:p.Trp858Cys
NM_001193640.1:c.3846G>T	NP_001180569.1:p.Trp1282Cys
NM_001257965.1:c.4110G>T	NP_001244894.1:p.Trp1370Cys
NM_001257966.1:c.2574G>T	NP_001244895.1:p.Trp858Cys
NM_201253.2:c.4182G>T	NP_957705.1:p.Trp1394Cys
NR_047563.1:n.4183G>T
NR_047564.1:n.4633G>T
XM_011509366.1:c.*287G>T	XP_011507668.1:n.*287G>T
XM_011509367.1:c.*161G>T	XP_011507669.1:n.*161G>T
XM_011509368.1:c.3600G>T	XP_011507670.1:p.Trp1200Cys
XM_011509369.1:c.2625G>T	XP_011507671.1:p.Trp875Cys
XM_011509369.2:c.2625G>T	XP_011507671.1:p.Trp875Cys
XM_017000851.1:c.3339G>T	XP_016856340.1:p.Trp1113Cys
XM_017000852.1:c.4317G>T	XP_016856341.1:p.Trp1439Cys
NM_201253.3:c.4182G>T MANE Select	NP_957705.1:p.Trp1394Cys
NM_001193640.2:c.3846G>T	NP_001180569.1:p.Trp1282Cys
NM_001257965.2:c.4110G>T	NP_001244894.1:p.Trp1370Cys
NR_047563.2:n.4135G>T
NR_047564.2:n.4585G>T
NM_001257966.2:c.2574G>T	NP_001244895.1:p.Trp858Cys