Canonical Allele Identifier: CA344035788

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446932A>C (hg19) ; chr1:g.197477802A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477802A>C , CM000663.2:g.197477802A>C	GRCh38
NC_000001.10:g.197446932A>C , CM000663.1:g.197446932A>C	GRCh37
NC_000001.9:g.195713555A>C	NCBI36
NG_008483.1:g.214525A>C
NG_008483.2:g.281341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4144A>C MANE Select	ENSP00000356370.3:p.Ser1382Arg
ENST00000367399.6:c.3808A>C	ENSP00000356369.2:p.Ser1270Arg
ENST00000367400.7:c.4144A>C	ENSP00000356370.3:p.Ser1382Arg
ENST00000448952.1:c.378A>C	ENSP00000395407.1:n.378A>C
ENST00000484075.5:c.*255A>C	ENSP00000433932.1:n.*255A>C
ENST00000535699.5:c.4072A>C	ENSP00000438786.1:p.Ser1358Arg
ENST00000538660.5:c.2536A>C	ENSP00000438091.1:p.Ser846Arg
NM_001193640.1:c.3808A>C	NP_001180569.1:p.Ser1270Arg
NM_001257965.1:c.4072A>C	NP_001244894.1:p.Ser1358Arg
NM_001257966.1:c.2536A>C	NP_001244895.1:p.Ser846Arg
NM_201253.2:c.4144A>C	NP_957705.1:p.Ser1382Arg
NR_047563.1:n.4145A>C
NR_047564.1:n.4595A>C
XM_011509366.1:c.*249A>C	XP_011507668.1:n.*249A>C
XM_011509367.1:c.*123A>C	XP_011507669.1:n.*123A>C
XM_011509368.1:c.3562A>C	XP_011507670.1:p.Ser1188Arg
XM_011509369.1:c.2587A>C	XP_011507671.1:p.Ser863Arg
XM_011509369.2:c.2587A>C	XP_011507671.1:p.Ser863Arg
XM_017000851.1:c.3301A>C	XP_016856340.1:p.Ser1101Arg
XM_017000852.1:c.4279A>C	XP_016856341.1:p.Ser1427Arg
NM_201253.3:c.4144A>C MANE Select	NP_957705.1:p.Ser1382Arg
NM_001193640.2:c.3808A>C	NP_001180569.1:p.Ser1270Arg
NM_001257965.2:c.4072A>C	NP_001244894.1:p.Ser1358Arg
NR_047563.2:n.4097A>C
NR_047564.2:n.4547A>C
NM_001257966.2:c.2536A>C	NP_001244895.1:p.Ser846Arg