Canonical Allele Identifier: CA344043255

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197403881T>G (hg19) ; chr1:g.197434751T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434751T>G , CM000663.2:g.197434751T>G	GRCh38
NC_000001.10:g.197403881T>G , CM000663.1:g.197403881T>G	GRCh37
NC_000001.9:g.195670504T>G	NCBI36
NG_008483.1:g.171474T>G
NG_008483.2:g.238290T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2888T>G MANE Select	ENSP00000356370.3:p.Phe963Cys
ENST00000638467.1:c.2888T>G	ENSP00000491102.1:p.Phe963Cys
ENST00000681519.1:c.1769T>G	ENSP00000505267.1:p.Phe590Cys
ENST00000367397.1:c.1031T>G	ENSP00000356367.1:p.Phe344Cys
ENST00000367399.6:c.2552T>G	ENSP00000356369.2:p.Phe851Cys
ENST00000367400.7:c.2888T>G	ENSP00000356370.3:p.Phe963Cys
ENST00000484075.5:c.2888T>G	ENSP00000433932.1:p.Phe963Cys
ENST00000535699.5:c.2816T>G	ENSP00000438786.1:p.Phe939Cys
ENST00000538660.5:c.2129-849T>G	ENSP00000438091.1:n.2129-849T>G
NM_001193640.1:c.2552T>G	NP_001180569.1:p.Phe851Cys
NM_001257965.1:c.2816T>G	NP_001244894.1:p.Phe939Cys
NM_001257966.1:c.2129-849T>G	NP_001244895.1:n.2129-849T>G
NM_201253.2:c.2888T>G	NP_957705.1:p.Phe963Cys
NR_047563.1:n.2889T>G
NR_047564.1:n.3097T>G
XM_011509365.1:c.2888T>G	XP_011507667.1:p.Phe963Cys
XM_011509366.1:c.2888T>G	XP_011507668.1:p.Phe963Cys
XM_011509367.1:c.2888T>G	XP_011507669.1:p.Phe963Cys
XM_011509368.1:c.2306T>G	XP_011507670.1:p.Phe769Cys
XM_011509369.1:c.1331T>G	XP_011507671.1:p.Phe444Cys
XM_011509365.2:c.2888T>G	XP_011507667.1:p.Phe963Cys
XM_011509369.2:c.1331T>G	XP_011507671.1:p.Phe444Cys
XM_017000851.1:c.2045T>G	XP_016856340.1:p.Phe682Cys
XM_017000852.1:c.3023T>G	XP_016856341.1:p.Phe1008Cys
NM_201253.3:c.2888T>G MANE Select	NP_957705.1:p.Phe963Cys
NM_001193640.2:c.2552T>G	NP_001180569.1:p.Phe851Cys
NM_001257965.2:c.2816T>G	NP_001244894.1:p.Phe939Cys
NR_047563.2:n.2841T>G
NR_047564.2:n.3049T>G
NM_001257966.2:c.2129-849T>G	NP_001244895.1:n.2129-849T>G