Canonical Allele Identifier: CA344038434

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197397047C>G (hg19) ; chr1:g.197427917C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427917C>G , CM000663.2:g.197427917C>G	GRCh38
NC_000001.10:g.197397047C>G , CM000663.1:g.197397047C>G	GRCh37
NC_000001.9:g.195663670C>G	NCBI36
NG_008483.1:g.164640C>G
NG_008483.2:g.231456C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2592C>G MANE Select	ENSP00000356370.3:p.Phe864Leu
ENST00000638467.1:c.2592C>G	ENSP00000491102.1:p.Phe864Leu
ENST00000681519.1:c.1473C>G	ENSP00000505267.1:p.Phe491Leu
ENST00000367397.1:c.735C>G	ENSP00000356367.1:p.Phe245Leu
ENST00000367399.6:c.2256C>G	ENSP00000356369.2:p.Phe752Leu
ENST00000367400.7:c.2592C>G	ENSP00000356370.3:p.Phe864Leu
ENST00000484075.5:c.2592C>G	ENSP00000433932.1:p.Phe864Leu
ENST00000535699.5:c.2385C>G	ENSP00000438786.1:p.Phe795Leu
ENST00000538660.5:c.2128+5961C>G	ENSP00000438091.1:n.2128+5961C>G
NM_001193640.1:c.2256C>G	NP_001180569.1:p.Phe752Leu
NM_001257965.1:c.2385C>G	NP_001244894.1:p.Phe795Leu
NM_001257966.1:c.2128+5961C>G	NP_001244895.1:n.2128+5961C>G
NM_201253.2:c.2592C>G	NP_957705.1:p.Phe864Leu
NR_047563.1:n.2593C>G
NR_047564.1:n.2801C>G
XM_011509365.1:c.2592C>G	XP_011507667.1:p.Phe864Leu
XM_011509366.1:c.2592C>G	XP_011507668.1:p.Phe864Leu
XM_011509367.1:c.2592C>G	XP_011507669.1:p.Phe864Leu
XM_011509368.1:c.2010C>G	XP_011507670.1:p.Phe670Leu
XM_011509369.1:c.1035C>G	XP_011507671.1:p.Phe345Leu
XM_011509365.2:c.2592C>G	XP_011507667.1:p.Phe864Leu
XM_011509369.2:c.1035C>G	XP_011507671.1:p.Phe345Leu
XM_017000851.1:c.1749C>G	XP_016856340.1:p.Phe583Leu
XM_017000852.1:c.2592C>G	XP_016856341.1:p.Phe864Leu
NM_201253.3:c.2592C>G MANE Select	NP_957705.1:p.Phe864Leu
NM_001193640.2:c.2256C>G	NP_001180569.1:p.Phe752Leu
NM_001257965.2:c.2385C>G	NP_001244894.1:p.Phe795Leu
NR_047563.2:n.2545C>G
NR_047564.2:n.2753C>G
NM_001257966.2:c.2128+5961C>G	NP_001244895.1:n.2128+5961C>G