Canonical Allele Identifier: CA344048058

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435323T>A , CM000663.2:g.197435323T>A	GRCh38
NC_000001.10:g.197404453T>A , CM000663.1:g.197404453T>A	GRCh37
NC_000001.9:g.195671076T>A	NCBI36
NG_008483.1:g.172046T>A
NG_008483.2:g.238862T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.3460T>A MANE Select	NP_957705.1:p.Cys1154Ser
ENST00000367400.8:c.3460T>A MANE Select	ENSP00000356370.3:p.Cys1154Ser
NM_001193640.1:c.3124T>A	NP_001180569.1:p.Cys1042Ser
NM_001193640.2:c.3124T>A	NP_001180569.1:p.Cys1042Ser
NM_001257965.1:c.3388T>A	NP_001244894.1:p.Cys1130Ser
NM_001257965.2:c.3388T>A	NP_001244894.1:p.Cys1130Ser
NM_001257966.1:c.2129-277T>A	NP_001244895.1:n.2129-277T>A
NM_001257966.2:c.2129-277T>A	NP_001244895.1:n.2129-277T>A
NM_201253.2:c.3460T>A	NP_957705.1:p.Cys1154Ser
NR_047563.1:n.3461T>A
NR_047563.2:n.3413T>A
NR_047564.1:n.3669T>A
NR_047564.2:n.3621T>A
ENST00000367397.1:c.1603T>A	ENSP00000356367.1:p.Cys535Ser
ENST00000367399.6:c.3124T>A	ENSP00000356369.2:p.Cys1042Ser
ENST00000367400.7:c.3460T>A	ENSP00000356370.3:p.Cys1154Ser
ENST00000484075.5:c.3460T>A	ENSP00000433932.1:p.Cys1154Ser
ENST00000535699.5:c.3388T>A	ENSP00000438786.1:p.Cys1130Ser
ENST00000538660.5:c.2129-277T>A	ENSP00000438091.1:n.2129-277T>A
ENST00000638467.1:c.3460T>A	ENSP00000491102.1:p.Cys1154Ser
ENST00000681519.1:c.2341T>A	ENSP00000505267.1:p.Cys781Ser
XM_011509365.1:c.3460T>A	XP_011507667.1:p.Cys1154Ser
XM_011509365.2:c.3460T>A	XP_011507667.1:p.Cys1154Ser
XM_011509366.1:c.3460T>A	XP_011507668.1:p.Cys1154Ser
XM_011509367.1:c.3460T>A	XP_011507669.1:p.Cys1154Ser
XM_011509368.1:c.2878T>A	XP_011507670.1:p.Cys960Ser
XM_011509369.1:c.1903T>A	XP_011507671.1:p.Cys635Ser
XM_011509369.2:c.1903T>A	XP_011507671.1:p.Cys635Ser
XM_017000851.1:c.2617T>A	XP_016856340.1:p.Cys873Ser
XM_017000852.1:c.3595T>A	XP_016856341.1:p.Cys1199Ser