Canonical Allele Identifier: CA422809260

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396819T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427689T>G , CM000663.2:g.197427689T>G	GRCh38
NC_000001.10:g.197396819T>G , CM000663.1:g.197396819T>G	GRCh37
NC_000001.9:g.195663442T>G	NCBI36
NG_008483.1:g.164412T>G
NG_008483.2:g.231228T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2364T>G MANE Select	ENSP00000356370.3:p.Leu788=
ENST00000638467.1:c.2364T>G	ENSP00000491102.1:p.Leu788=
ENST00000681519.1:c.1245T>G	ENSP00000505267.1:p.Leu415=
ENST00000367397.1:c.507T>G	ENSP00000356367.1:p.Leu169=
ENST00000367399.6:c.2028T>G	ENSP00000356369.2:p.Leu676=
ENST00000367400.7:c.2364T>G	ENSP00000356370.3:p.Leu788=
ENST00000480086.2:n.265T>G
ENST00000484075.5:c.2364T>G	ENSP00000433932.1:p.Leu788=
ENST00000535699.5:c.2157T>G	ENSP00000438786.1:p.Leu719=
ENST00000538660.5:c.2128+5733T>G	ENSP00000438091.1:n.2128+5733T>G
NM_001193640.1:c.2028T>G	NP_001180569.1:p.Leu676=
NM_001257965.1:c.2157T>G	NP_001244894.1:p.Leu719=
NM_001257966.1:c.2128+5733T>G	NP_001244895.1:n.2128+5733T>G
NM_201253.2:c.2364T>G	NP_957705.1:p.Leu788=
NR_047563.1:n.2365T>G
NR_047564.1:n.2573T>G
XM_011509365.1:c.2364T>G	XP_011507667.1:p.Leu788=
XM_011509366.1:c.2364T>G	XP_011507668.1:p.Leu788=
XM_011509367.1:c.2364T>G	XP_011507669.1:p.Leu788=
XM_011509368.1:c.1782T>G	XP_011507670.1:p.Leu594=
XM_011509369.1:c.807T>G	XP_011507671.1:p.Leu269=
XM_011509365.2:c.2364T>G	XP_011507667.1:p.Leu788=
XM_011509369.2:c.807T>G	XP_011507671.1:p.Leu269=
XM_017000851.1:c.1521T>G	XP_016856340.1:p.Leu507=
XM_017000852.1:c.2364T>G	XP_016856341.1:p.Leu788=
NM_201253.3:c.2364T>G MANE Select	NP_957705.1:p.Leu788=
NM_001193640.2:c.2028T>G	NP_001180569.1:p.Leu676=
NM_001257965.2:c.2157T>G	NP_001244894.1:p.Leu719=
NR_047563.2:n.2317T>G
NR_047564.2:n.2525T>G
NM_001257966.2:c.2128+5733T>G	NP_001244895.1:n.2128+5733T>G