Canonical Allele Identifier: CA344032149

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421528G>A , CM000663.2:g.197421528G>A	GRCh38
NC_000001.10:g.197390658G>A , CM000663.1:g.197390658G>A	GRCh37
NC_000001.9:g.195657281G>A	NCBI36
NG_008483.1:g.158251G>A
NG_008483.2:g.225067G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.1700G>A MANE Select	NP_957705.1:p.Trp567Ter
ENST00000367400.8:c.1700G>A MANE Select	ENSP00000356370.3:p.Trp567Ter
NM_001193640.1:c.1364G>A	NP_001180569.1:p.Trp455Ter
NM_001193640.2:c.1364G>A	NP_001180569.1:p.Trp455Ter
NM_001257965.1:c.1493G>A	NP_001244894.1:p.Trp498Ter
NM_001257965.2:c.1493G>A	NP_001244894.1:p.Trp498Ter
NM_001257966.1:c.1700G>A	NP_001244895.1:p.Trp567Ter
NM_001257966.2:c.1700G>A	NP_001244895.1:p.Trp567Ter
NM_201253.2:c.1700G>A	NP_957705.1:p.Trp567Ter
NR_047563.1:n.1909G>A
NR_047563.2:n.1861G>A
NR_047564.1:n.1909G>A
NR_047564.2:n.1861G>A
ENST00000367397.1:c.-158G>A	ENSP00000356367.1:n.-158G>A
ENST00000367399.6:c.1364G>A	ENSP00000356369.2:p.Trp455Ter
ENST00000367400.7:c.1700G>A	ENSP00000356370.3:p.Trp567Ter
ENST00000484075.5:c.1700G>A	ENSP00000433932.1:p.Trp567Ter
ENST00000535699.5:c.1493G>A	ENSP00000438786.1:p.Trp498Ter
ENST00000538660.5:c.1700G>A	ENSP00000438091.1:p.Trp567Ter
ENST00000638467.1:c.1700G>A	ENSP00000491102.1:p.Trp567Ter
ENST00000681519.1:c.581G>A	ENSP00000505267.1:p.Trp194Ter
XM_011509365.1:c.1700G>A	XP_011507667.1:p.Trp567Ter
XM_011509365.2:c.1700G>A	XP_011507667.1:p.Trp567Ter
XM_011509366.1:c.1700G>A	XP_011507668.1:p.Trp567Ter
XM_011509367.1:c.1700G>A	XP_011507669.1:p.Trp567Ter
XM_011509368.1:c.1118G>A	XP_011507670.1:p.Trp373Ter
XM_011509369.1:c.143G>A	XP_011507671.1:p.Trp48Ter
XM_011509369.2:c.143G>A	XP_011507671.1:p.Trp48Ter
XM_017000851.1:c.857G>A	XP_016856340.1:p.Trp286Ter
XM_017000852.1:c.1700G>A	XP_016856341.1:p.Trp567Ter