Canonical Allele Identifier: CA422808843

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396954T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427824T>G , CM000663.2:g.197427824T>G	GRCh38
NC_000001.10:g.197396954T>G , CM000663.1:g.197396954T>G	GRCh37
NC_000001.9:g.195663577T>G	NCBI36
NG_008483.1:g.164547T>G
NG_008483.2:g.231363T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2499T>G MANE Select	ENSP00000356370.3:p.Gly833=
ENST00000638467.1:c.2499T>G	ENSP00000491102.1:p.Gly833=
ENST00000681519.1:c.1380T>G	ENSP00000505267.1:p.Gly460=
ENST00000367397.1:c.642T>G	ENSP00000356367.1:p.Gly214=
ENST00000367399.6:c.2163T>G	ENSP00000356369.2:p.Gly721=
ENST00000367400.7:c.2499T>G	ENSP00000356370.3:p.Gly833=
ENST00000480086.2:n.400T>G
ENST00000484075.5:c.2499T>G	ENSP00000433932.1:p.Gly833=
ENST00000535699.5:c.2292T>G	ENSP00000438786.1:p.Gly764=
ENST00000538660.5:c.2128+5868T>G	ENSP00000438091.1:n.2128+5868T>G
NM_001193640.1:c.2163T>G	NP_001180569.1:p.Gly721=
NM_001257965.1:c.2292T>G	NP_001244894.1:p.Gly764=
NM_001257966.1:c.2128+5868T>G	NP_001244895.1:n.2128+5868T>G
NM_201253.2:c.2499T>G	NP_957705.1:p.Gly833=
NR_047563.1:n.2500T>G
NR_047564.1:n.2708T>G
XM_011509365.1:c.2499T>G	XP_011507667.1:p.Gly833=
XM_011509366.1:c.2499T>G	XP_011507668.1:p.Gly833=
XM_011509367.1:c.2499T>G	XP_011507669.1:p.Gly833=
XM_011509368.1:c.1917T>G	XP_011507670.1:p.Gly639=
XM_011509369.1:c.942T>G	XP_011507671.1:p.Gly314=
XM_011509365.2:c.2499T>G	XP_011507667.1:p.Gly833=
XM_011509369.2:c.942T>G	XP_011507671.1:p.Gly314=
XM_017000851.1:c.1656T>G	XP_016856340.1:p.Gly552=
XM_017000852.1:c.2499T>G	XP_016856341.1:p.Gly833=
NM_201253.3:c.2499T>G MANE Select	NP_957705.1:p.Gly833=
NM_001193640.2:c.2163T>G	NP_001180569.1:p.Gly721=
NM_001257965.2:c.2292T>G	NP_001244894.1:p.Gly764=
NR_047563.2:n.2452T>G
NR_047564.2:n.2660T>G
NM_001257966.2:c.2128+5868T>G	NP_001244895.1:n.2128+5868T>G