Canonical Allele Identifier: CA344032994

Gene: CRB1

Linked Data

• COSMIC: COSM3481076
• MyVariant Identifiers: chr1:g.197390900A>G (hg19) ; chr1:g.197421770A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421770A>G , CM000663.2:g.197421770A>G	GRCh38
NC_000001.10:g.197390900A>G , CM000663.1:g.197390900A>G	GRCh37
NC_000001.9:g.195657523A>G	NCBI36
NG_008483.1:g.158493A>G
NG_008483.2:g.225309A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1942A>G MANE Select	ENSP00000356370.3:p.Ile648Val
ENST00000638467.1:c.1942A>G	ENSP00000491102.1:p.Ile648Val
ENST00000681519.1:c.823A>G	ENSP00000505267.1:p.Ile275Val
ENST00000367397.1:c.85A>G	ENSP00000356367.1:p.Ile29Val
ENST00000367399.6:c.1606A>G	ENSP00000356369.2:p.Ile536Val
ENST00000367400.7:c.1942A>G	ENSP00000356370.3:p.Ile648Val
ENST00000484075.5:c.1942A>G	ENSP00000433932.1:p.Ile648Val
ENST00000535699.5:c.1735A>G	ENSP00000438786.1:p.Ile579Val
ENST00000538660.5:c.1942A>G	ENSP00000438091.1:p.Ile648Val
NM_001193640.1:c.1606A>G	NP_001180569.1:p.Ile536Val
NM_001257965.1:c.1735A>G	NP_001244894.1:p.Ile579Val
NM_001257966.1:c.1942A>G	NP_001244895.1:p.Ile648Val
NM_201253.2:c.1942A>G	NP_957705.1:p.Ile648Val
NR_047563.1:n.1943A>G
NR_047564.1:n.2151A>G
XM_011509365.1:c.1942A>G	XP_011507667.1:p.Ile648Val
XM_011509366.1:c.1942A>G	XP_011507668.1:p.Ile648Val
XM_011509367.1:c.1942A>G	XP_011507669.1:p.Ile648Val
XM_011509368.1:c.1360A>G	XP_011507670.1:p.Ile454Val
XM_011509369.1:c.385A>G	XP_011507671.1:p.Ile129Val
XM_011509365.2:c.1942A>G	XP_011507667.1:p.Ile648Val
XM_011509369.2:c.385A>G	XP_011507671.1:p.Ile129Val
XM_017000851.1:c.1099A>G	XP_016856340.1:p.Ile367Val
XM_017000852.1:c.1942A>G	XP_016856341.1:p.Ile648Val
NM_201253.3:c.1942A>G MANE Select	NP_957705.1:p.Ile648Val
NM_001193640.2:c.1606A>G	NP_001180569.1:p.Ile536Val
NM_001257965.2:c.1735A>G	NP_001244894.1:p.Ile579Val
NR_047563.2:n.1895A>G
NR_047564.2:n.2103A>G
NM_001257966.2:c.1942A>G	NP_001244895.1:p.Ile648Val