Canonical Allele Identifier: CA344037076

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396829A>G (hg19) ; chr1:g.197427699A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427699A>G , CM000663.2:g.197427699A>G	GRCh38
NC_000001.10:g.197396829A>G , CM000663.1:g.197396829A>G	GRCh37
NC_000001.9:g.195663452A>G	NCBI36
NG_008483.1:g.164422A>G
NG_008483.2:g.231238A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2374A>G MANE Select	ENSP00000356370.3:p.Asn792Asp
ENST00000638467.1:c.2374A>G	ENSP00000491102.1:p.Asn792Asp
ENST00000681519.1:c.1255A>G	ENSP00000505267.1:p.Asn419Asp
ENST00000367397.1:c.517A>G	ENSP00000356367.1:p.Asn173Asp
ENST00000367399.6:c.2038A>G	ENSP00000356369.2:p.Asn680Asp
ENST00000367400.7:c.2374A>G	ENSP00000356370.3:p.Asn792Asp
ENST00000480086.2:n.275A>G
ENST00000484075.5:c.2374A>G	ENSP00000433932.1:p.Asn792Asp
ENST00000535699.5:c.2167A>G	ENSP00000438786.1:p.Asn723Asp
ENST00000538660.5:c.2128+5743A>G	ENSP00000438091.1:n.2128+5743A>G
NM_001193640.1:c.2038A>G	NP_001180569.1:p.Asn680Asp
NM_001257965.1:c.2167A>G	NP_001244894.1:p.Asn723Asp
NM_001257966.1:c.2128+5743A>G	NP_001244895.1:n.2128+5743A>G
NM_201253.2:c.2374A>G	NP_957705.1:p.Asn792Asp
NR_047563.1:n.2375A>G
NR_047564.1:n.2583A>G
XM_011509365.1:c.2374A>G	XP_011507667.1:p.Asn792Asp
XM_011509366.1:c.2374A>G	XP_011507668.1:p.Asn792Asp
XM_011509367.1:c.2374A>G	XP_011507669.1:p.Asn792Asp
XM_011509368.1:c.1792A>G	XP_011507670.1:p.Asn598Asp
XM_011509369.1:c.817A>G	XP_011507671.1:p.Asn273Asp
XM_011509365.2:c.2374A>G	XP_011507667.1:p.Asn792Asp
XM_011509369.2:c.817A>G	XP_011507671.1:p.Asn273Asp
XM_017000851.1:c.1531A>G	XP_016856340.1:p.Asn511Asp
XM_017000852.1:c.2374A>G	XP_016856341.1:p.Asn792Asp
NM_201253.3:c.2374A>G MANE Select	NP_957705.1:p.Asn792Asp
NM_001193640.2:c.2038A>G	NP_001180569.1:p.Asn680Asp
NM_001257965.2:c.2167A>G	NP_001244894.1:p.Asn723Asp
NR_047563.2:n.2327A>G
NR_047564.2:n.2535A>G
NM_001257966.2:c.2128+5743A>G	NP_001244895.1:n.2128+5743A>G