Canonical Allele Identifier: CA422672259

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197398599A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197429469A>T , CM000663.2:g.197429469A>T	GRCh38
NC_000001.10:g.197398599A>T , CM000663.1:g.197398599A>T	GRCh37
NC_000001.9:g.195665222A>T	NCBI36
NG_008483.1:g.166192A>T
NG_008483.2:g.233008A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2697A>T MANE Select	ENSP00000356370.3:p.Gly899=
ENST00000638467.1:c.2697A>T	ENSP00000491102.1:p.Gly899=
ENST00000681519.1:c.1578A>T	ENSP00000505267.1:p.Gly526=
ENST00000367397.1:c.840A>T	ENSP00000356367.1:p.Gly280=
ENST00000367399.6:c.2361A>T	ENSP00000356369.2:p.Gly787=
ENST00000367400.7:c.2697A>T	ENSP00000356370.3:p.Gly899=
ENST00000484075.5:c.2697A>T	ENSP00000433932.1:p.Gly899=
ENST00000535699.5:c.2625A>T	ENSP00000438786.1:p.Gly875=
ENST00000538660.5:c.2129-6131A>T	ENSP00000438091.1:n.2129-6131A>T
NM_001193640.1:c.2361A>T	NP_001180569.1:p.Gly787=
NM_001257965.1:c.2625A>T	NP_001244894.1:p.Gly875=
NM_001257966.1:c.2129-6131A>T	NP_001244895.1:n.2129-6131A>T
NM_201253.2:c.2697A>T	NP_957705.1:p.Gly899=
NR_047563.1:n.2698A>T
NR_047564.1:n.2906A>T
XM_011509365.1:c.2697A>T	XP_011507667.1:p.Gly899=
XM_011509366.1:c.2697A>T	XP_011507668.1:p.Gly899=
XM_011509367.1:c.2697A>T	XP_011507669.1:p.Gly899=
XM_011509368.1:c.2115A>T	XP_011507670.1:p.Gly705=
XM_011509369.1:c.1140A>T	XP_011507671.1:p.Gly380=
XM_011509365.2:c.2697A>T	XP_011507667.1:p.Gly899=
XM_011509369.2:c.1140A>T	XP_011507671.1:p.Gly380=
XM_017000851.1:c.1854A>T	XP_016856340.1:p.Gly618=
XM_017000852.1:c.2832A>T	XP_016856341.1:p.Gly944=
NM_201253.3:c.2697A>T MANE Select	NP_957705.1:p.Gly899=
NM_001193640.2:c.2361A>T	NP_001180569.1:p.Gly787=
NM_001257965.2:c.2625A>T	NP_001244894.1:p.Gly875=
NR_047563.2:n.2650A>T
NR_047564.2:n.2858A>T
NM_001257966.2:c.2129-6131A>T	NP_001244895.1:n.2129-6131A>T