Canonical Allele Identifier: CA422808830

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396945C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427815C>T , CM000663.2:g.197427815C>T	GRCh38
NC_000001.10:g.197396945C>T , CM000663.1:g.197396945C>T	GRCh37
NC_000001.9:g.195663568C>T	NCBI36
NG_008483.1:g.164538C>T
NG_008483.2:g.231354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2490C>T MANE Select	ENSP00000356370.3:p.Ile830=
ENST00000638467.1:c.2490C>T	ENSP00000491102.1:p.Ile830=
ENST00000681519.1:c.1371C>T	ENSP00000505267.1:p.Ile457=
ENST00000367397.1:c.633C>T	ENSP00000356367.1:p.Ile211=
ENST00000367399.6:c.2154C>T	ENSP00000356369.2:p.Ile718=
ENST00000367400.7:c.2490C>T	ENSP00000356370.3:p.Ile830=
ENST00000480086.2:n.391C>T
ENST00000484075.5:c.2490C>T	ENSP00000433932.1:p.Ile830=
ENST00000535699.5:c.2283C>T	ENSP00000438786.1:p.Ile761=
ENST00000538660.5:c.2128+5859C>T	ENSP00000438091.1:n.2128+5859C>T
NM_001193640.1:c.2154C>T	NP_001180569.1:p.Ile718=
NM_001257965.1:c.2283C>T	NP_001244894.1:p.Ile761=
NM_001257966.1:c.2128+5859C>T	NP_001244895.1:n.2128+5859C>T
NM_201253.2:c.2490C>T	NP_957705.1:p.Ile830=
NR_047563.1:n.2491C>T
NR_047564.1:n.2699C>T
XM_011509365.1:c.2490C>T	XP_011507667.1:p.Ile830=
XM_011509366.1:c.2490C>T	XP_011507668.1:p.Ile830=
XM_011509367.1:c.2490C>T	XP_011507669.1:p.Ile830=
XM_011509368.1:c.1908C>T	XP_011507670.1:p.Ile636=
XM_011509369.1:c.933C>T	XP_011507671.1:p.Ile311=
XM_011509365.2:c.2490C>T	XP_011507667.1:p.Ile830=
XM_011509369.2:c.933C>T	XP_011507671.1:p.Ile311=
XM_017000851.1:c.1647C>T	XP_016856340.1:p.Ile549=
XM_017000852.1:c.2490C>T	XP_016856341.1:p.Ile830=
NM_201253.3:c.2490C>T MANE Select	NP_957705.1:p.Ile830=
NM_001193640.2:c.2154C>T	NP_001180569.1:p.Ile718=
NM_001257965.2:c.2283C>T	NP_001244894.1:p.Ile761=
NR_047563.2:n.2443C>T
NR_047564.2:n.2651C>T
NM_001257966.2:c.2128+5859C>T	NP_001244895.1:n.2128+5859C>T