Canonical Allele Identifier: CA344047027

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197404295A>G (hg19) ; chr1:g.197435165A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435165A>G , CM000663.2:g.197435165A>G	GRCh38
NC_000001.10:g.197404295A>G , CM000663.1:g.197404295A>G	GRCh37
NC_000001.9:g.195670918A>G	NCBI36
NG_008483.1:g.171888A>G
NG_008483.2:g.238704A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367400.8:c.3302A>G MANE Select	ENSP00000356370.3:p.Glu1101Gly
ENST00000638467.1:c.3302A>G	ENSP00000491102.1:p.Glu1101Gly
ENST00000681519.1:c.2183A>G	ENSP00000505267.1:p.Glu728Gly
ENST00000367397.1:c.1445A>G	ENSP00000356367.1:p.Glu482Gly
ENST00000367399.6:c.2966A>G	ENSP00000356369.2:p.Glu989Gly
ENST00000367400.7:c.3302A>G	ENSP00000356370.3:p.Glu1101Gly
ENST00000484075.5:c.3302A>G	ENSP00000433932.1:p.Glu1101Gly
ENST00000535699.5:c.3230A>G	ENSP00000438786.1:p.Glu1077Gly
ENST00000538660.5:c.2129-435A>G	ENSP00000438091.1:n.2129-435A>G
NM_001193640.1:c.2966A>G	NP_001180569.1:p.Glu989Gly
NM_001257965.1:c.3230A>G	NP_001244894.1:p.Glu1077Gly
NM_001257966.1:c.2129-435A>G	NP_001244895.1:n.2129-435A>G
NM_201253.2:c.3302A>G	NP_957705.1:p.Glu1101Gly
NR_047563.1:n.3303A>G
NR_047564.1:n.3511A>G
XM_011509365.1:c.3302A>G	XP_011507667.1:p.Glu1101Gly
XM_011509366.1:c.3302A>G	XP_011507668.1:p.Glu1101Gly
XM_011509367.1:c.3302A>G	XP_011507669.1:p.Glu1101Gly
XM_011509368.1:c.2720A>G	XP_011507670.1:p.Glu907Gly
XM_011509369.1:c.1745A>G	XP_011507671.1:p.Glu582Gly
XM_011509365.2:c.3302A>G	XP_011507667.1:p.Glu1101Gly
XM_011509369.2:c.1745A>G	XP_011507671.1:p.Glu582Gly
XM_017000851.1:c.2459A>G	XP_016856340.1:p.Glu820Gly
XM_017000852.1:c.3437A>G	XP_016856341.1:p.Glu1146Gly
NM_201253.3:c.3302A>G MANE Select	NP_957705.1:p.Glu1101Gly
NM_001193640.2:c.2966A>G	NP_001180569.1:p.Glu989Gly
NM_001257965.2:c.3230A>G	NP_001244894.1:p.Glu1077Gly
NR_047563.2:n.3255A>G
NR_047564.2:n.3463A>G
NM_001257966.2:c.2129-435A>G	NP_001244895.1:n.2129-435A>G