Canonical Allele Identifier: CA344048065

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197435324G>C , CM000663.2:g.197435324G>C	GRCh38
NC_000001.10:g.197404454G>C , CM000663.1:g.197404454G>C	GRCh37
NC_000001.9:g.195671077G>C	NCBI36
NG_008483.1:g.172047G>C
NG_008483.2:g.238863G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_201253.3:c.3461G>C MANE Select	NP_957705.1:p.Cys1154Ser
ENST00000367400.8:c.3461G>C MANE Select	ENSP00000356370.3:p.Cys1154Ser
NM_001193640.1:c.3125G>C	NP_001180569.1:p.Cys1042Ser
NM_001193640.2:c.3125G>C	NP_001180569.1:p.Cys1042Ser
NM_001257965.1:c.3389G>C	NP_001244894.1:p.Cys1130Ser
NM_001257965.2:c.3389G>C	NP_001244894.1:p.Cys1130Ser
NM_001257966.1:c.2129-276G>C	NP_001244895.1:n.2129-276G>C
NM_001257966.2:c.2129-276G>C	NP_001244895.1:n.2129-276G>C
NM_201253.2:c.3461G>C	NP_957705.1:p.Cys1154Ser
NR_047563.1:n.3462G>C
NR_047563.2:n.3414G>C
NR_047564.1:n.3670G>C
NR_047564.2:n.3622G>C
ENST00000367397.1:c.1604G>C	ENSP00000356367.1:p.Cys535Ser
ENST00000367399.6:c.3125G>C	ENSP00000356369.2:p.Cys1042Ser
ENST00000367400.7:c.3461G>C	ENSP00000356370.3:p.Cys1154Ser
ENST00000484075.5:c.3461G>C	ENSP00000433932.1:p.Cys1154Ser
ENST00000535699.5:c.3389G>C	ENSP00000438786.1:p.Cys1130Ser
ENST00000538660.5:c.2129-276G>C	ENSP00000438091.1:n.2129-276G>C
ENST00000638467.1:c.3461G>C	ENSP00000491102.1:p.Cys1154Ser
ENST00000681519.1:c.2342G>C	ENSP00000505267.1:p.Cys781Ser
XM_011509365.1:c.3461G>C	XP_011507667.1:p.Cys1154Ser
XM_011509365.2:c.3461G>C	XP_011507667.1:p.Cys1154Ser
XM_011509366.1:c.3461G>C	XP_011507668.1:p.Cys1154Ser
XM_011509367.1:c.3461G>C	XP_011507669.1:p.Cys1154Ser
XM_011509368.1:c.2879G>C	XP_011507670.1:p.Cys960Ser
XM_011509369.1:c.1904G>C	XP_011507671.1:p.Cys635Ser
XM_011509369.2:c.1904G>C	XP_011507671.1:p.Cys635Ser
XM_017000851.1:c.2618G>C	XP_016856340.1:p.Cys873Ser
XM_017000852.1:c.3596G>C	XP_016856341.1:p.Cys1199Ser