Canonical Allele Identifier: CA344035514

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446851T>G (hg19) ; chr1:g.197477721T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477721T>G , CM000663.2:g.197477721T>G	GRCh38
NC_000001.10:g.197446851T>G , CM000663.1:g.197446851T>G	GRCh37
NC_000001.9:g.195713474T>G	NCBI36
NG_008483.1:g.214444T>G
NG_008483.2:g.281260T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4063T>G MANE Select	ENSP00000356370.3:p.Leu1355Val
ENST00000367399.6:c.3727T>G	ENSP00000356369.2:p.Leu1243Val
ENST00000367400.7:c.4063T>G	ENSP00000356370.3:p.Leu1355Val
ENST00000448952.1:c.297T>G	ENSP00000395407.1:n.297T>G
ENST00000484075.5:c.*174T>G	ENSP00000433932.1:n.*174T>G
ENST00000535699.5:c.3991T>G	ENSP00000438786.1:p.Leu1331Val
ENST00000538660.5:c.2455T>G	ENSP00000438091.1:p.Leu819Val
NM_001193640.1:c.3727T>G	NP_001180569.1:p.Leu1243Val
NM_001257965.1:c.3991T>G	NP_001244894.1:p.Leu1331Val
NM_001257966.1:c.2455T>G	NP_001244895.1:p.Leu819Val
NM_201253.2:c.4063T>G	NP_957705.1:p.Leu1355Val
NR_047563.1:n.4064T>G
NR_047564.1:n.4514T>G
XM_011509366.1:c.*168T>G	XP_011507668.1:n.*168T>G
XM_011509367.1:c.*42T>G	XP_011507669.1:n.*42T>G
XM_011509368.1:c.3481T>G	XP_011507670.1:p.Leu1161Val
XM_011509369.1:c.2506T>G	XP_011507671.1:p.Leu836Val
XM_011509369.2:c.2506T>G	XP_011507671.1:p.Leu836Val
XM_017000851.1:c.3220T>G	XP_016856340.1:p.Leu1074Val
XM_017000852.1:c.4198T>G	XP_016856341.1:p.Leu1400Val
NM_201253.3:c.4063T>G MANE Select	NP_957705.1:p.Leu1355Val
NM_001193640.2:c.3727T>G	NP_001180569.1:p.Leu1243Val
NM_001257965.2:c.3991T>G	NP_001244894.1:p.Leu1331Val
NR_047563.2:n.4016T>G
NR_047564.2:n.4466T>G
NM_001257966.2:c.2455T>G	NP_001244895.1:p.Leu819Val