Canonical Allele Identifier: CA344035533

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446860A>G (hg19) ; chr1:g.197477730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477730A>G , CM000663.2:g.197477730A>G	GRCh38
NC_000001.10:g.197446860A>G , CM000663.1:g.197446860A>G	GRCh37
NC_000001.9:g.195713483A>G	NCBI36
NG_008483.1:g.214453A>G
NG_008483.2:g.281269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4072A>G MANE Select	ENSP00000356370.3:p.Ile1358Val
ENST00000367399.6:c.3736A>G	ENSP00000356369.2:p.Ile1246Val
ENST00000367400.7:c.4072A>G	ENSP00000356370.3:p.Ile1358Val
ENST00000448952.1:c.306A>G	ENSP00000395407.1:n.306A>G
ENST00000484075.5:c.*183A>G	ENSP00000433932.1:n.*183A>G
ENST00000535699.5:c.4000A>G	ENSP00000438786.1:p.Ile1334Val
ENST00000538660.5:c.2464A>G	ENSP00000438091.1:p.Ile822Val
NM_001193640.1:c.3736A>G	NP_001180569.1:p.Ile1246Val
NM_001257965.1:c.4000A>G	NP_001244894.1:p.Ile1334Val
NM_001257966.1:c.2464A>G	NP_001244895.1:p.Ile822Val
NM_201253.2:c.4072A>G	NP_957705.1:p.Ile1358Val
NR_047563.1:n.4073A>G
NR_047564.1:n.4523A>G
XM_011509366.1:c.*177A>G	XP_011507668.1:n.*177A>G
XM_011509367.1:c.*51A>G	XP_011507669.1:n.*51A>G
XM_011509368.1:c.3490A>G	XP_011507670.1:p.Ile1164Val
XM_011509369.1:c.2515A>G	XP_011507671.1:p.Ile839Val
XM_011509369.2:c.2515A>G	XP_011507671.1:p.Ile839Val
XM_017000851.1:c.3229A>G	XP_016856340.1:p.Ile1077Val
XM_017000852.1:c.4207A>G	XP_016856341.1:p.Ile1403Val
NM_201253.3:c.4072A>G MANE Select	NP_957705.1:p.Ile1358Val
NM_001193640.2:c.3736A>G	NP_001180569.1:p.Ile1246Val
NM_001257965.2:c.4000A>G	NP_001244894.1:p.Ile1334Val
NR_047563.2:n.4025A>G
NR_047564.2:n.4475A>G
NM_001257966.2:c.2464A>G	NP_001244895.1:p.Ile822Val