Canonical Allele Identifier: CA422723837

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197298075G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197328945G>A , CM000663.2:g.197328945G>A	GRCh38
NC_000001.10:g.197298075G>A , CM000663.1:g.197298075G>A	GRCh37
NC_000001.9:g.195564698G>A	NCBI36
NG_008483.1:g.65668G>A
NG_008483.2:g.132484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.594G>A MANE Select	ENSP00000356370.3:p.Glu198=
ENST00000638467.1:c.594G>A	ENSP00000491102.1:p.Glu198=
ENST00000367399.6:c.594G>A	ENSP00000356369.2:p.Glu198=
ENST00000367400.7:c.594G>A	ENSP00000356370.3:p.Glu198=
ENST00000475659.1:n.731G>A
ENST00000484075.5:c.594G>A	ENSP00000433932.1:p.Glu198=
ENST00000535699.5:c.387G>A	ENSP00000438786.1:p.Glu129=
ENST00000538660.5:c.594G>A	ENSP00000438091.1:p.Glu198=
NM_001193640.1:c.594G>A	NP_001180569.1:p.Glu198=
NM_001257965.1:c.387G>A	NP_001244894.1:p.Glu129=
NM_001257966.1:c.594G>A	NP_001244895.1:p.Glu198=
NM_201253.2:c.594G>A	NP_957705.1:p.Glu198=
NR_047563.1:n.803G>A
NR_047564.1:n.803G>A
XM_011509365.1:c.594G>A	XP_011507667.1:p.Glu198=
XM_011509366.1:c.594G>A	XP_011507668.1:p.Glu198=
XM_011509367.1:c.594G>A	XP_011507669.1:p.Glu198=
XM_011509368.1:c.71-15336G>A	XP_011507670.1:n.71-15336G>A
XM_011509365.2:c.594G>A	XP_011507667.1:p.Glu198=
XM_017000851.1:c.-110G>A	XP_016856340.1:n.-110G>A
XM_017000852.1:c.594G>A	XP_016856341.1:p.Glu198=
NM_201253.3:c.594G>A MANE Select	NP_957705.1:p.Glu198=
NM_001193640.2:c.594G>A	NP_001180569.1:p.Glu198=
NM_001257965.2:c.387G>A	NP_001244894.1:p.Glu129=
NR_047563.2:n.755G>A
NR_047564.2:n.755G>A
NM_001257966.2:c.594G>A	NP_001244895.1:p.Glu198=