Canonical Allele Identifier: CA1312440

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197442168G>A , CM000663.2:g.197442168G>A	GRCh38
NC_000001.10:g.197411298G>A , CM000663.1:g.197411298G>A	GRCh37
NC_000001.9:g.195677921G>A	NCBI36
NG_008483.1:g.178891G>A
NG_008483.2:g.245707G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.3881G>A MANE Select	NP_957705.1:p.Cys1294Tyr
ENST00000367400.8:c.3881G>A MANE Select	ENSP00000356370.3:p.Cys1294Tyr
NM_001193640.1:c.3545G>A	NP_001180569.1:p.Cys1182Tyr
NM_001193640.2:c.3545G>A	NP_001180569.1:p.Cys1182Tyr
NM_001257965.1:c.3809G>A	NP_001244894.1:p.Cys1270Tyr
NM_001257965.2:c.3809G>A	NP_001244894.1:p.Cys1270Tyr
NM_001257966.1:c.2273G>A	NP_001244895.1:p.Cys758Tyr
NM_001257966.2:c.2273G>A	NP_001244895.1:p.Cys758Tyr
NM_201253.2:c.3881G>A	NP_957705.1:p.Cys1294Tyr
NR_047563.1:n.3882G>A
NR_047563.2:n.3834G>A
NR_047564.1:n.4090G>A
NR_047564.2:n.4042G>A
ENST00000367397.1:c.*3489G>A	ENSP00000356367.1:n.*3489G>A
ENST00000367399.6:c.3545G>A	ENSP00000356369.2:p.Cys1182Tyr
ENST00000367400.7:c.3881G>A	ENSP00000356370.3:p.Cys1294Tyr
ENST00000484075.5:c.3881G>A	ENSP00000433932.1:p.Cys1294Tyr
ENST00000535699.5:c.3809G>A	ENSP00000438786.1:p.Cys1270Tyr
ENST00000538660.5:c.2273G>A	ENSP00000438091.1:p.Cys758Tyr
ENST00000638467.1:c.3881G>A	ENSP00000491102.1:p.Cys1294Tyr
ENST00000681519.1:c.2762G>A	ENSP00000505267.1:p.Cys921Tyr
XM_011509365.1:c.3881G>A	XP_011507667.1:p.Cys1294Tyr
XM_011509365.2:c.3881G>A	XP_011507667.1:p.Cys1294Tyr
XM_011509366.1:c.3881G>A	XP_011507668.1:p.Cys1294Tyr
XM_011509367.1:c.3878+3493G>A	XP_011507669.1:n.3878+3493G>A
XM_011509368.1:c.3299G>A	XP_011507670.1:p.Cys1100Tyr
XM_011509369.1:c.2324G>A	XP_011507671.1:p.Cys775Tyr
XM_011509369.2:c.2324G>A	XP_011507671.1:p.Cys775Tyr
XM_017000851.1:c.3038G>A	XP_016856340.1:p.Cys1013Tyr
XM_017000852.1:c.4016G>A	XP_016856341.1:p.Cys1339Tyr