Canonical Allele Identifier: CA344036625

Gene: CRB1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197427531A>T , CM000663.2:g.197427531A>T	GRCh38
NC_000001.10:g.197396661A>T , CM000663.1:g.197396661A>T	GRCh37
NC_000001.9:g.195663284A>T	NCBI36
NG_008483.1:g.164254A>T
NG_008483.2:g.231070A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2206A>T MANE Select	ENSP00000356370.3:p.Thr736Ser
ENST00000638467.1:c.2206A>T	ENSP00000491102.1:p.Thr736Ser
ENST00000681519.1:c.1087A>T	ENSP00000505267.1:p.Thr363Ser
ENST00000367397.1:c.349A>T	ENSP00000356367.1:p.Thr117Ser
ENST00000367399.6:c.1870A>T	ENSP00000356369.2:p.Thr624Ser
ENST00000367400.7:c.2206A>T	ENSP00000356370.3:p.Thr736Ser
ENST00000480086.2:n.107A>T
ENST00000484075.5:c.2206A>T	ENSP00000433932.1:p.Thr736Ser
ENST00000535699.5:c.1999A>T	ENSP00000438786.1:p.Thr667Ser
ENST00000538660.5:c.2128+5575A>T	ENSP00000438091.1:n.2128+5575A>T
NM_001193640.1:c.1870A>T	NP_001180569.1:p.Thr624Ser
NM_001257965.1:c.1999A>T	NP_001244894.1:p.Thr667Ser
NM_001257966.1:c.2128+5575A>T	NP_001244895.1:n.2128+5575A>T
NM_201253.2:c.2206A>T	NP_957705.1:p.Thr736Ser
NR_047563.1:n.2207A>T
NR_047564.1:n.2415A>T
XM_011509365.1:c.2206A>T	XP_011507667.1:p.Thr736Ser
XM_011509366.1:c.2206A>T	XP_011507668.1:p.Thr736Ser
XM_011509367.1:c.2206A>T	XP_011507669.1:p.Thr736Ser
XM_011509368.1:c.1624A>T	XP_011507670.1:p.Thr542Ser
XM_011509369.1:c.649A>T	XP_011507671.1:p.Thr217Ser
XM_011509365.2:c.2206A>T	XP_011507667.1:p.Thr736Ser
XM_011509369.2:c.649A>T	XP_011507671.1:p.Thr217Ser
XM_017000851.1:c.1363A>T	XP_016856340.1:p.Thr455Ser
XM_017000852.1:c.2206A>T	XP_016856341.1:p.Thr736Ser
NM_201253.3:c.2206A>T MANE Select	NP_957705.1:p.Thr736Ser
NM_001193640.2:c.1870A>T	NP_001180569.1:p.Thr624Ser
NM_001257965.2:c.1999A>T	NP_001244894.1:p.Thr667Ser
NR_047563.2:n.2159A>T
NR_047564.2:n.2367A>T
NM_001257966.2:c.2128+5575A>T	NP_001244895.1:n.2128+5575A>T