Canonical Allele Identifier: CA344035520

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446854T>A (hg19) ; chr1:g.197477724T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477724T>A , CM000663.2:g.197477724T>A	GRCh38
NC_000001.10:g.197446854T>A , CM000663.1:g.197446854T>A	GRCh37
NC_000001.9:g.195713477T>A	NCBI36
NG_008483.1:g.214447T>A
NG_008483.2:g.281263T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.4066T>A MANE Select	ENSP00000356370.3:p.Leu1356Ile
ENST00000367399.6:c.3730T>A	ENSP00000356369.2:p.Leu1244Ile
ENST00000367400.7:c.4066T>A	ENSP00000356370.3:p.Leu1356Ile
ENST00000448952.1:c.300T>A	ENSP00000395407.1:n.300T>A
ENST00000484075.5:c.*177T>A	ENSP00000433932.1:n.*177T>A
ENST00000535699.5:c.3994T>A	ENSP00000438786.1:p.Leu1332Ile
ENST00000538660.5:c.2458T>A	ENSP00000438091.1:p.Leu820Ile
NM_001193640.1:c.3730T>A	NP_001180569.1:p.Leu1244Ile
NM_001257965.1:c.3994T>A	NP_001244894.1:p.Leu1332Ile
NM_001257966.1:c.2458T>A	NP_001244895.1:p.Leu820Ile
NM_201253.2:c.4066T>A	NP_957705.1:p.Leu1356Ile
NR_047563.1:n.4067T>A
NR_047564.1:n.4517T>A
XM_011509366.1:c.*171T>A	XP_011507668.1:n.*171T>A
XM_011509367.1:c.*45T>A	XP_011507669.1:n.*45T>A
XM_011509368.1:c.3484T>A	XP_011507670.1:p.Leu1162Ile
XM_011509369.1:c.2509T>A	XP_011507671.1:p.Leu837Ile
XM_011509369.2:c.2509T>A	XP_011507671.1:p.Leu837Ile
XM_017000851.1:c.3223T>A	XP_016856340.1:p.Leu1075Ile
XM_017000852.1:c.4201T>A	XP_016856341.1:p.Leu1401Ile
NM_201253.3:c.4066T>A MANE Select	NP_957705.1:p.Leu1356Ile
NM_001193640.2:c.3730T>A	NP_001180569.1:p.Leu1244Ile
NM_001257965.2:c.3994T>A	NP_001244894.1:p.Leu1332Ile
NR_047563.2:n.4019T>A
NR_047564.2:n.4469T>A
NM_001257966.2:c.2458T>A	NP_001244895.1:p.Leu820Ile