Canonical Allele Identifier: CA422808712

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396852A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427722A>G , CM000663.2:g.197427722A>G	GRCh38
NC_000001.10:g.197396852A>G , CM000663.1:g.197396852A>G	GRCh37
NC_000001.9:g.195663475A>G	NCBI36
NG_008483.1:g.164445A>G
NG_008483.2:g.231261A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2397A>G MANE Select	ENSP00000356370.3:p.Lys799=
ENST00000638467.1:c.2397A>G	ENSP00000491102.1:p.Lys799=
ENST00000681519.1:c.1278A>G	ENSP00000505267.1:p.Lys426=
ENST00000367397.1:c.540A>G	ENSP00000356367.1:p.Lys180=
ENST00000367399.6:c.2061A>G	ENSP00000356369.2:p.Lys687=
ENST00000367400.7:c.2397A>G	ENSP00000356370.3:p.Lys799=
ENST00000480086.2:n.298A>G
ENST00000484075.5:c.2397A>G	ENSP00000433932.1:p.Lys799=
ENST00000535699.5:c.2190A>G	ENSP00000438786.1:p.Lys730=
ENST00000538660.5:c.2128+5766A>G	ENSP00000438091.1:n.2128+5766A>G
NM_001193640.1:c.2061A>G	NP_001180569.1:p.Lys687=
NM_001257965.1:c.2190A>G	NP_001244894.1:p.Lys730=
NM_001257966.1:c.2128+5766A>G	NP_001244895.1:n.2128+5766A>G
NM_201253.2:c.2397A>G	NP_957705.1:p.Lys799=
NR_047563.1:n.2398A>G
NR_047564.1:n.2606A>G
XM_011509365.1:c.2397A>G	XP_011507667.1:p.Lys799=
XM_011509366.1:c.2397A>G	XP_011507668.1:p.Lys799=
XM_011509367.1:c.2397A>G	XP_011507669.1:p.Lys799=
XM_011509368.1:c.1815A>G	XP_011507670.1:p.Lys605=
XM_011509369.1:c.840A>G	XP_011507671.1:p.Lys280=
XM_011509365.2:c.2397A>G	XP_011507667.1:p.Lys799=
XM_011509369.2:c.840A>G	XP_011507671.1:p.Lys280=
XM_017000851.1:c.1554A>G	XP_016856340.1:p.Lys518=
XM_017000852.1:c.2397A>G	XP_016856341.1:p.Lys799=
NM_201253.3:c.2397A>G MANE Select	NP_957705.1:p.Lys799=
NM_001193640.2:c.2061A>G	NP_001180569.1:p.Lys687=
NM_001257965.2:c.2190A>G	NP_001244894.1:p.Lys730=
NR_047563.2:n.2350A>G
NR_047564.2:n.2558A>G
NM_001257966.2:c.2128+5766A>G	NP_001244895.1:n.2128+5766A>G