Canonical Allele Identifier: CA344038064

Gene: CRB1

Linked Data

• gnomAD v4: 1-197427856-A-G
• MyVariant Identifiers: chr1:g.197396986A>G (hg19) ; chr1:g.197427856A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427856A>G , CM000663.2:g.197427856A>G	GRCh38
NC_000001.10:g.197396986A>G , CM000663.1:g.197396986A>G	GRCh37
NC_000001.9:g.195663609A>G	NCBI36
NG_008483.1:g.164579A>G
NG_008483.2:g.231395A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2531A>G MANE Select	ENSP00000356370.3:p.Asn844Ser
ENST00000638467.1:c.2531A>G	ENSP00000491102.1:p.Asn844Ser
ENST00000681519.1:c.1412A>G	ENSP00000505267.1:p.Asn471Ser
ENST00000367397.1:c.674A>G	ENSP00000356367.1:p.Asn225Ser
ENST00000367399.6:c.2195A>G	ENSP00000356369.2:p.Asn732Ser
ENST00000367400.7:c.2531A>G	ENSP00000356370.3:p.Asn844Ser
ENST00000484075.5:c.2531A>G	ENSP00000433932.1:p.Asn844Ser
ENST00000535699.5:c.2324A>G	ENSP00000438786.1:p.Asn775Ser
ENST00000538660.5:c.2128+5900A>G	ENSP00000438091.1:n.2128+5900A>G
NM_001193640.1:c.2195A>G	NP_001180569.1:p.Asn732Ser
NM_001257965.1:c.2324A>G	NP_001244894.1:p.Asn775Ser
NM_001257966.1:c.2128+5900A>G	NP_001244895.1:n.2128+5900A>G
NM_201253.2:c.2531A>G	NP_957705.1:p.Asn844Ser
NR_047563.1:n.2532A>G
NR_047564.1:n.2740A>G
XM_011509365.1:c.2531A>G	XP_011507667.1:p.Asn844Ser
XM_011509366.1:c.2531A>G	XP_011507668.1:p.Asn844Ser
XM_011509367.1:c.2531A>G	XP_011507669.1:p.Asn844Ser
XM_011509368.1:c.1949A>G	XP_011507670.1:p.Asn650Ser
XM_011509369.1:c.974A>G	XP_011507671.1:p.Asn325Ser
XM_011509365.2:c.2531A>G	XP_011507667.1:p.Asn844Ser
XM_011509369.2:c.974A>G	XP_011507671.1:p.Asn325Ser
XM_017000851.1:c.1688A>G	XP_016856340.1:p.Asn563Ser
XM_017000852.1:c.2531A>G	XP_016856341.1:p.Asn844Ser
NM_201253.3:c.2531A>G MANE Select	NP_957705.1:p.Asn844Ser
NM_001193640.2:c.2195A>G	NP_001180569.1:p.Asn732Ser
NM_001257965.2:c.2324A>G	NP_001244894.1:p.Asn775Ser
NR_047563.2:n.2484A>G
NR_047564.2:n.2692A>G
NM_001257966.2:c.2128+5900A>G	NP_001244895.1:n.2128+5900A>G