Canonical Allele Identifier: CA422677509

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446854T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4066T>C MANE Select	ENSP00000356370.3:p.Leu1356=
ENST00000367399.6:c.3730T>C	ENSP00000356369.2:p.Leu1244=
ENST00000367400.7:c.4066T>C	ENSP00000356370.3:p.Leu1356=
ENST00000448952.1:c.300T>C	ENSP00000395407.1:n.300T>C
ENST00000484075.5:c.*177T>C	ENSP00000433932.1:n.*177T>C
ENST00000535699.5:c.3994T>C	ENSP00000438786.1:p.Leu1332=
ENST00000538660.5:c.2458T>C	ENSP00000438091.1:p.Leu820=
NM_001193640.1:c.3730T>C	NP_001180569.1:p.Leu1244=
NM_001257965.1:c.3994T>C	NP_001244894.1:p.Leu1332=
NM_001257966.1:c.2458T>C	NP_001244895.1:p.Leu820=
NM_201253.2:c.4066T>C	NP_957705.1:p.Leu1356=
NR_047563.1:n.4067T>C
NR_047564.1:n.4517T>C
XM_011509366.1:c.*171T>C	XP_011507668.1:n.*171T>C
XM_011509367.1:c.*45T>C	XP_011507669.1:n.*45T>C
XM_011509368.1:c.3484T>C	XP_011507670.1:p.Leu1162=
XM_011509369.1:c.2509T>C	XP_011507671.1:p.Leu837=
XM_011509369.2:c.2509T>C	XP_011507671.1:p.Leu837=
XM_017000851.1:c.3223T>C	XP_016856340.1:p.Leu1075=
XM_017000852.1:c.4201T>C	XP_016856341.1:p.Leu1401=
NM_201253.3:c.4066T>C MANE Select	NP_957705.1:p.Leu1356=
NM_001193640.2:c.3730T>C	NP_001180569.1:p.Leu1244=
NM_001257965.2:c.3994T>C	NP_001244894.1:p.Leu1332=
NR_047563.2:n.4019T>C
NR_047564.2:n.4469T>C
NM_001257966.2:c.2458T>C	NP_001244895.1:p.Leu820=