Canonical Allele Identifier: CA344035436

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197446811C>G (hg19) ; chr1:g.197477681C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197477681C>G , CM000663.2:g.197477681C>G	GRCh38
NC_000001.10:g.197446811C>G , CM000663.1:g.197446811C>G	GRCh37
NC_000001.9:g.195713434C>G	NCBI36
NG_008483.1:g.214404C>G
NG_008483.2:g.281220C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.4023C>G MANE Select	ENSP00000356370.3:p.Ile1341Met
ENST00000367399.6:c.3687C>G	ENSP00000356369.2:p.Ile1229Met
ENST00000367400.7:c.4023C>G	ENSP00000356370.3:p.Ile1341Met
ENST00000448952.1:c.257C>G	ENSP00000395407.1:n.257C>G
ENST00000484075.5:c.*134C>G	ENSP00000433932.1:n.*134C>G
ENST00000535699.5:c.3951C>G	ENSP00000438786.1:p.Ile1317Met
ENST00000538660.5:c.2415C>G	ENSP00000438091.1:p.Ile805Met
NM_001193640.1:c.3687C>G	NP_001180569.1:p.Ile1229Met
NM_001257965.1:c.3951C>G	NP_001244894.1:p.Ile1317Met
NM_001257966.1:c.2415C>G	NP_001244895.1:p.Ile805Met
NM_201253.2:c.4023C>G	NP_957705.1:p.Ile1341Met
NR_047563.1:n.4024C>G
NR_047564.1:n.4474C>G
XM_011509366.1:c.*128C>G	XP_011507668.1:n.*128C>G
XM_011509367.1:c.*2C>G	XP_011507669.1:n.*2C>G
XM_011509368.1:c.3441C>G	XP_011507670.1:p.Ile1147Met
XM_011509369.1:c.2466C>G	XP_011507671.1:p.Ile822Met
XM_011509369.2:c.2466C>G	XP_011507671.1:p.Ile822Met
XM_017000851.1:c.3180C>G	XP_016856340.1:p.Ile1060Met
XM_017000852.1:c.4158C>G	XP_016856341.1:p.Ile1386Met
NM_201253.3:c.4023C>G MANE Select	NP_957705.1:p.Ile1341Met
NM_001193640.2:c.3687C>G	NP_001180569.1:p.Ile1229Met
NM_001257965.2:c.3951C>G	NP_001244894.1:p.Ile1317Met
NR_047563.2:n.3976C>G
NR_047564.2:n.4426C>G
NM_001257966.2:c.2415C>G	NP_001244895.1:p.Ile805Met