Canonical Allele Identifier: CA422808431

Gene: CRB1

Linked Data

• ClinVar Variation Id: 1146322
• ClinVar RCV Id: RCV001485487
• dbSNP Id: rs1350306887
• gnomAD v4: 1-197421598-A-G
• MyVariant Identifiers: chr1:g.197390728A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421598A>G , CM000663.2:g.197421598A>G	GRCh38
NC_000001.10:g.197390728A>G , CM000663.1:g.197390728A>G	GRCh37
NC_000001.9:g.195657351A>G	NCBI36
NG_008483.1:g.158321A>G
NG_008483.2:g.225137A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1770A>G MANE Select	ENSP00000356370.3:p.Lys590=
ENST00000638467.1:c.1770A>G	ENSP00000491102.1:p.Lys590=
ENST00000681519.1:c.651A>G	ENSP00000505267.1:p.Lys217=
ENST00000367397.1:c.-88A>G	ENSP00000356367.1:n.-88A>G
ENST00000367399.6:c.1434A>G	ENSP00000356369.2:p.Lys478=
ENST00000367400.7:c.1770A>G	ENSP00000356370.3:p.Lys590=
ENST00000484075.5:c.1770A>G	ENSP00000433932.1:p.Lys590=
ENST00000535699.5:c.1563A>G	ENSP00000438786.1:p.Lys521=
ENST00000538660.5:c.1770A>G	ENSP00000438091.1:p.Lys590=
NM_001193640.1:c.1434A>G	NP_001180569.1:p.Lys478=
NM_001257965.1:c.1563A>G	NP_001244894.1:p.Lys521=
NM_001257966.1:c.1770A>G	NP_001244895.1:p.Lys590=
NM_201253.2:c.1770A>G	NP_957705.1:p.Lys590=
NR_047563.1:n.1922+57A>G
NR_047564.1:n.1979A>G
XM_011509365.1:c.1770A>G	XP_011507667.1:p.Lys590=
XM_011509366.1:c.1770A>G	XP_011507668.1:p.Lys590=
XM_011509367.1:c.1770A>G	XP_011507669.1:p.Lys590=
XM_011509368.1:c.1188A>G	XP_011507670.1:p.Lys396=
XM_011509369.1:c.213A>G	XP_011507671.1:p.Lys71=
XM_011509365.2:c.1770A>G	XP_011507667.1:p.Lys590=
XM_011509369.2:c.213A>G	XP_011507671.1:p.Lys71=
XM_017000851.1:c.927A>G	XP_016856340.1:p.Lys309=
XM_017000852.1:c.1770A>G	XP_016856341.1:p.Lys590=
NM_201253.3:c.1770A>G MANE Select	NP_957705.1:p.Lys590=
NM_001193640.2:c.1434A>G	NP_001180569.1:p.Lys478=
NM_001257965.2:c.1563A>G	NP_001244894.1:p.Lys521=
NR_047563.2:n.1874+57A>G
NR_047564.2:n.1931A>G
NM_001257966.2:c.1770A>G	NP_001244895.1:p.Lys590=