Canonical Allele Identifier: CA344035457

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446821T>G (hg19) ; chr1:g.197477691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477691T>G , CM000663.2:g.197477691T>G	GRCh38
NC_000001.10:g.197446821T>G , CM000663.1:g.197446821T>G	GRCh37
NC_000001.9:g.195713444T>G	NCBI36
NG_008483.1:g.214414T>G
NG_008483.2:g.281230T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4033T>G MANE Select	ENSP00000356370.3:p.Phe1345Val
ENST00000367399.6:c.3697T>G	ENSP00000356369.2:p.Phe1233Val
ENST00000367400.7:c.4033T>G	ENSP00000356370.3:p.Phe1345Val
ENST00000448952.1:c.267T>G	ENSP00000395407.1:n.267T>G
ENST00000484075.5:c.*144T>G	ENSP00000433932.1:n.*144T>G
ENST00000535699.5:c.3961T>G	ENSP00000438786.1:p.Phe1321Val
ENST00000538660.5:c.2425T>G	ENSP00000438091.1:p.Phe809Val
NM_001193640.1:c.3697T>G	NP_001180569.1:p.Phe1233Val
NM_001257965.1:c.3961T>G	NP_001244894.1:p.Phe1321Val
NM_001257966.1:c.2425T>G	NP_001244895.1:p.Phe809Val
NM_201253.2:c.4033T>G	NP_957705.1:p.Phe1345Val
NR_047563.1:n.4034T>G
NR_047564.1:n.4484T>G
XM_011509366.1:c.*138T>G	XP_011507668.1:n.*138T>G
XM_011509367.1:c.*12T>G	XP_011507669.1:n.*12T>G
XM_011509368.1:c.3451T>G	XP_011507670.1:p.Phe1151Val
XM_011509369.1:c.2476T>G	XP_011507671.1:p.Phe826Val
XM_011509369.2:c.2476T>G	XP_011507671.1:p.Phe826Val
XM_017000851.1:c.3190T>G	XP_016856340.1:p.Phe1064Val
XM_017000852.1:c.4168T>G	XP_016856341.1:p.Phe1390Val
NM_201253.3:c.4033T>G MANE Select	NP_957705.1:p.Phe1345Val
NM_001193640.2:c.3697T>G	NP_001180569.1:p.Phe1233Val
NM_001257965.2:c.3961T>G	NP_001244894.1:p.Phe1321Val
NR_047563.2:n.3986T>G
NR_047564.2:n.4436T>G
NM_001257966.2:c.2425T>G	NP_001244895.1:p.Phe809Val