Canonical Allele Identifier: CA344032586

Gene: CRB1

Linked Data

• COSMIC: COSM2125562 ; COSM4228557
• MyVariant Identifiers: chr1:g.197390730G>A (hg19) ; chr1:g.197421600G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421600G>A , CM000663.2:g.197421600G>A	GRCh38
NC_000001.10:g.197390730G>A , CM000663.1:g.197390730G>A	GRCh37
NC_000001.9:g.195657353G>A	NCBI36
NG_008483.1:g.158323G>A
NG_008483.2:g.225139G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1772G>A MANE Select	ENSP00000356370.3:p.Cys591Tyr
ENST00000638467.1:c.1772G>A	ENSP00000491102.1:p.Cys591Tyr
ENST00000681519.1:c.653G>A	ENSP00000505267.1:p.Cys218Tyr
ENST00000367397.1:c.-86G>A	ENSP00000356367.1:n.-86G>A
ENST00000367399.6:c.1436G>A	ENSP00000356369.2:p.Cys479Tyr
ENST00000367400.7:c.1772G>A	ENSP00000356370.3:p.Cys591Tyr
ENST00000484075.5:c.1772G>A	ENSP00000433932.1:p.Cys591Tyr
ENST00000535699.5:c.1565G>A	ENSP00000438786.1:p.Cys522Tyr
ENST00000538660.5:c.1772G>A	ENSP00000438091.1:p.Cys591Tyr
NM_001193640.1:c.1436G>A	NP_001180569.1:p.Cys479Tyr
NM_001257965.1:c.1565G>A	NP_001244894.1:p.Cys522Tyr
NM_001257966.1:c.1772G>A	NP_001244895.1:p.Cys591Tyr
NM_201253.2:c.1772G>A	NP_957705.1:p.Cys591Tyr
NR_047563.1:n.1922+59G>A
NR_047564.1:n.1981G>A
XM_011509365.1:c.1772G>A	XP_011507667.1:p.Cys591Tyr
XM_011509366.1:c.1772G>A	XP_011507668.1:p.Cys591Tyr
XM_011509367.1:c.1772G>A	XP_011507669.1:p.Cys591Tyr
XM_011509368.1:c.1190G>A	XP_011507670.1:p.Cys397Tyr
XM_011509369.1:c.215G>A	XP_011507671.1:p.Cys72Tyr
XM_011509365.2:c.1772G>A	XP_011507667.1:p.Cys591Tyr
XM_011509369.2:c.215G>A	XP_011507671.1:p.Cys72Tyr
XM_017000851.1:c.929G>A	XP_016856340.1:p.Cys310Tyr
XM_017000852.1:c.1772G>A	XP_016856341.1:p.Cys591Tyr
NM_201253.3:c.1772G>A MANE Select	NP_957705.1:p.Cys591Tyr
NM_001193640.2:c.1436G>A	NP_001180569.1:p.Cys479Tyr
NM_001257965.2:c.1565G>A	NP_001244894.1:p.Cys522Tyr
NR_047563.2:n.1874+59G>A
NR_047564.2:n.1933G>A
NM_001257966.2:c.1772G>A	NP_001244895.1:p.Cys591Tyr