Canonical Allele Identifier: CA344032682

Gene: CRB1

Linked Data

• ClinVar Variation Id: 973939
• ClinVar RCV Id: RCV001250655
• dbSNP Id: rs371114178
• MyVariant Identifiers: chr1:g.197390776T>A (hg19) ; chr1:g.197421646T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421646T>A , CM000663.2:g.197421646T>A	GRCh38
NC_000001.10:g.197390776T>A , CM000663.1:g.197390776T>A	GRCh37
NC_000001.9:g.195657399T>A	NCBI36
NG_008483.1:g.158369T>A
NG_008483.2:g.225185T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1818T>A MANE Select	ENSP00000356370.3:p.Cys606Ter
ENST00000638467.1:c.1818T>A	ENSP00000491102.1:p.Cys606Ter
ENST00000681519.1:c.699T>A	ENSP00000505267.1:p.Cys233Ter
ENST00000367397.1:c.-40T>A	ENSP00000356367.1:n.-40T>A
ENST00000367399.6:c.1482T>A	ENSP00000356369.2:p.Cys494Ter
ENST00000367400.7:c.1818T>A	ENSP00000356370.3:p.Cys606Ter
ENST00000484075.5:c.1818T>A	ENSP00000433932.1:p.Cys606Ter
ENST00000535699.5:c.1611T>A	ENSP00000438786.1:p.Cys537Ter
ENST00000538660.5:c.1818T>A	ENSP00000438091.1:p.Cys606Ter
NM_001193640.1:c.1482T>A	NP_001180569.1:p.Cys494Ter
NM_001257965.1:c.1611T>A	NP_001244894.1:p.Cys537Ter
NM_001257966.1:c.1818T>A	NP_001244895.1:p.Cys606Ter
NM_201253.2:c.1818T>A	NP_957705.1:p.Cys606Ter
NR_047563.1:n.1923-104T>A
NR_047564.1:n.2027T>A
XM_011509365.1:c.1818T>A	XP_011507667.1:p.Cys606Ter
XM_011509366.1:c.1818T>A	XP_011507668.1:p.Cys606Ter
XM_011509367.1:c.1818T>A	XP_011507669.1:p.Cys606Ter
XM_011509368.1:c.1236T>A	XP_011507670.1:p.Cys412Ter
XM_011509369.1:c.261T>A	XP_011507671.1:p.Cys87Ter
XM_011509365.2:c.1818T>A	XP_011507667.1:p.Cys606Ter
XM_011509369.2:c.261T>A	XP_011507671.1:p.Cys87Ter
XM_017000851.1:c.975T>A	XP_016856340.1:p.Cys325Ter
XM_017000852.1:c.1818T>A	XP_016856341.1:p.Cys606Ter
NM_201253.3:c.1818T>A MANE Select	NP_957705.1:p.Cys606Ter
NM_001193640.2:c.1482T>A	NP_001180569.1:p.Cys494Ter
NM_001257965.2:c.1611T>A	NP_001244894.1:p.Cys537Ter
NR_047563.2:n.1875-104T>A
NR_047564.2:n.1979T>A
NM_001257966.2:c.1818T>A	NP_001244895.1:p.Cys606Ter