Canonical Allele Identifier: CA422808263

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197390495A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421365A>C , CM000663.2:g.197421365A>C	GRCh38
NC_000001.10:g.197390495A>C , CM000663.1:g.197390495A>C	GRCh37
NC_000001.9:g.195657118A>C	NCBI36
NG_008483.1:g.158088A>C
NG_008483.2:g.224904A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.1537A>C MANE Select	ENSP00000356370.3:p.Arg513=
ENST00000638467.1:c.1537A>C	ENSP00000491102.1:p.Arg513=
ENST00000681519.1:c.418A>C	ENSP00000505267.1:p.Arg140=
ENST00000367397.1:c.-321A>C	ENSP00000356367.1:n.-321A>C
ENST00000367399.6:c.1201A>C	ENSP00000356369.2:p.Arg401=
ENST00000367400.7:c.1537A>C	ENSP00000356370.3:p.Arg513=
ENST00000476483.1:n.497A>C
ENST00000484075.5:c.1537A>C	ENSP00000433932.1:p.Arg513=
ENST00000535699.5:c.1330A>C	ENSP00000438786.1:p.Arg444=
ENST00000538660.5:c.1537A>C	ENSP00000438091.1:p.Arg513=
NM_001193640.1:c.1201A>C	NP_001180569.1:p.Arg401=
NM_001257965.1:c.1330A>C	NP_001244894.1:p.Arg444=
NM_001257966.1:c.1537A>C	NP_001244895.1:p.Arg513=
NM_201253.2:c.1537A>C	NP_957705.1:p.Arg513=
NR_047563.1:n.1746A>C
NR_047564.1:n.1746A>C
XM_011509365.1:c.1537A>C	XP_011507667.1:p.Arg513=
XM_011509366.1:c.1537A>C	XP_011507668.1:p.Arg513=
XM_011509367.1:c.1537A>C	XP_011507669.1:p.Arg513=
XM_011509368.1:c.955A>C	XP_011507670.1:p.Arg319=
XM_011509369.1:c.-21A>C	XP_011507671.1:n.-21A>C
XM_011509365.2:c.1537A>C	XP_011507667.1:p.Arg513=
XM_011509369.2:c.-21A>C	XP_011507671.1:n.-21A>C
XM_017000851.1:c.694A>C	XP_016856340.1:p.Arg232=
XM_017000852.1:c.1537A>C	XP_016856341.1:p.Arg513=
NM_201253.3:c.1537A>C MANE Select	NP_957705.1:p.Arg513=
NM_001193640.2:c.1201A>C	NP_001180569.1:p.Arg401=
NM_001257965.2:c.1330A>C	NP_001244894.1:p.Arg444=
NR_047563.2:n.1698A>C
NR_047564.2:n.1698A>C
NM_001257966.2:c.1537A>C	NP_001244895.1:p.Arg513=