Canonical Allele Identifier: CA344037140

Gene: CRB1

Linked Data

• MyVariant Identifiers: chr1:g.197396853A>T (hg19) ; chr1:g.197427723A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427723A>T , CM000663.2:g.197427723A>T	GRCh38
NC_000001.10:g.197396853A>T , CM000663.1:g.197396853A>T	GRCh37
NC_000001.9:g.195663476A>T	NCBI36
NG_008483.1:g.164446A>T
NG_008483.2:g.231262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2398A>T MANE Select	ENSP00000356370.3:p.Ile800Phe
ENST00000638467.1:c.2398A>T	ENSP00000491102.1:p.Ile800Phe
ENST00000681519.1:c.1279A>T	ENSP00000505267.1:p.Ile427Phe
ENST00000367397.1:c.541A>T	ENSP00000356367.1:p.Ile181Phe
ENST00000367399.6:c.2062A>T	ENSP00000356369.2:p.Ile688Phe
ENST00000367400.7:c.2398A>T	ENSP00000356370.3:p.Ile800Phe
ENST00000480086.2:n.299A>T
ENST00000484075.5:c.2398A>T	ENSP00000433932.1:p.Ile800Phe
ENST00000535699.5:c.2191A>T	ENSP00000438786.1:p.Ile731Phe
ENST00000538660.5:c.2128+5767A>T	ENSP00000438091.1:n.2128+5767A>T
NM_001193640.1:c.2062A>T	NP_001180569.1:p.Ile688Phe
NM_001257965.1:c.2191A>T	NP_001244894.1:p.Ile731Phe
NM_001257966.1:c.2128+5767A>T	NP_001244895.1:n.2128+5767A>T
NM_201253.2:c.2398A>T	NP_957705.1:p.Ile800Phe
NR_047563.1:n.2399A>T
NR_047564.1:n.2607A>T
XM_011509365.1:c.2398A>T	XP_011507667.1:p.Ile800Phe
XM_011509366.1:c.2398A>T	XP_011507668.1:p.Ile800Phe
XM_011509367.1:c.2398A>T	XP_011507669.1:p.Ile800Phe
XM_011509368.1:c.1816A>T	XP_011507670.1:p.Ile606Phe
XM_011509369.1:c.841A>T	XP_011507671.1:p.Ile281Phe
XM_011509365.2:c.2398A>T	XP_011507667.1:p.Ile800Phe
XM_011509369.2:c.841A>T	XP_011507671.1:p.Ile281Phe
XM_017000851.1:c.1555A>T	XP_016856340.1:p.Ile519Phe
XM_017000852.1:c.2398A>T	XP_016856341.1:p.Ile800Phe
NM_201253.3:c.2398A>T MANE Select	NP_957705.1:p.Ile800Phe
NM_001193640.2:c.2062A>T	NP_001180569.1:p.Ile688Phe
NM_001257965.2:c.2191A>T	NP_001244894.1:p.Ile731Phe
NR_047563.2:n.2351A>T
NR_047564.2:n.2559A>T
NM_001257966.2:c.2128+5767A>T	NP_001244895.1:n.2128+5767A>T