Canonical Allele Identifier: CA344037846

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396958C>A (hg19) ; chr1:g.197427828C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427828C>A , CM000663.2:g.197427828C>A	GRCh38
NC_000001.10:g.197396958C>A , CM000663.1:g.197396958C>A	GRCh37
NC_000001.9:g.195663581C>A	NCBI36
NG_008483.1:g.164551C>A
NG_008483.2:g.231367C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.2503C>A MANE Select	ENSP00000356370.3:p.Leu835Ile
ENST00000638467.1:c.2503C>A	ENSP00000491102.1:p.Leu835Ile
ENST00000681519.1:c.1384C>A	ENSP00000505267.1:p.Leu462Ile
ENST00000367397.1:c.646C>A	ENSP00000356367.1:p.Leu216Ile
ENST00000367399.6:c.2167C>A	ENSP00000356369.2:p.Leu723Ile
ENST00000367400.7:c.2503C>A	ENSP00000356370.3:p.Leu835Ile
ENST00000480086.2:n.404C>A
ENST00000484075.5:c.2503C>A	ENSP00000433932.1:p.Leu835Ile
ENST00000535699.5:c.2296C>A	ENSP00000438786.1:p.Leu766Ile
ENST00000538660.5:c.2128+5872C>A	ENSP00000438091.1:n.2128+5872C>A
NM_001193640.1:c.2167C>A	NP_001180569.1:p.Leu723Ile
NM_001257965.1:c.2296C>A	NP_001244894.1:p.Leu766Ile
NM_001257966.1:c.2128+5872C>A	NP_001244895.1:n.2128+5872C>A
NM_201253.2:c.2503C>A	NP_957705.1:p.Leu835Ile
NR_047563.1:n.2504C>A
NR_047564.1:n.2712C>A
XM_011509365.1:c.2503C>A	XP_011507667.1:p.Leu835Ile
XM_011509366.1:c.2503C>A	XP_011507668.1:p.Leu835Ile
XM_011509367.1:c.2503C>A	XP_011507669.1:p.Leu835Ile
XM_011509368.1:c.1921C>A	XP_011507670.1:p.Leu641Ile
XM_011509369.1:c.946C>A	XP_011507671.1:p.Leu316Ile
XM_011509365.2:c.2503C>A	XP_011507667.1:p.Leu835Ile
XM_011509369.2:c.946C>A	XP_011507671.1:p.Leu316Ile
XM_017000851.1:c.1660C>A	XP_016856340.1:p.Leu554Ile
XM_017000852.1:c.2503C>A	XP_016856341.1:p.Leu835Ile
NM_201253.3:c.2503C>A MANE Select	NP_957705.1:p.Leu835Ile
NM_001193640.2:c.2167C>A	NP_001180569.1:p.Leu723Ile
NM_001257965.2:c.2296C>A	NP_001244894.1:p.Leu766Ile
NR_047563.2:n.2456C>A
NR_047564.2:n.2664C>A
NM_001257966.2:c.2128+5872C>A	NP_001244895.1:n.2128+5872C>A