Canonical Allele Identifier: CA1218068660

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197434772C= , CM000663.2:g.197434772C=	GRCh38
NC_000001.10:g.197403902C= , CM000663.1:g.197403902C=	GRCh37
NC_000001.9:g.195670525C=	NCBI36
NG_008483.1:g.171495C=
NG_008483.2:g.238311C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.2909C= MANE Select	ENSP00000356370.3:p.Thr970=
ENST00000638467.1:c.2909C=	ENSP00000491102.1:p.Thr970=
ENST00000681519.1:c.1790C=	ENSP00000505267.1:p.Thr597=
ENST00000367397.1:c.1052C=	ENSP00000356367.1:p.Thr351=
ENST00000367399.6:c.2573C=	ENSP00000356369.2:p.Thr858=
ENST00000367400.7:c.2909C=	ENSP00000356370.3:p.Thr970=
ENST00000484075.5:c.2909C=	ENSP00000433932.1:p.Thr970=
ENST00000535699.5:c.2837C=	ENSP00000438786.1:p.Thr946=
ENST00000538660.5:c.2129-828C=	ENSP00000438091.1:n.2129-828C=
NM_001193640.1:c.2573C=	NP_001180569.1:p.Thr858=
NM_001257965.1:c.2837C=	NP_001244894.1:p.Thr946=
NM_001257966.1:c.2129-828C=	NP_001244895.1:n.2129-828C=
NM_201253.2:c.2909C=	NP_957705.1:p.Thr970=
NR_047563.1:n.2910C=
NR_047564.1:n.3118C=
XM_011509365.1:c.2909C=	XP_011507667.1:p.Thr970=
XM_011509366.1:c.2909C=	XP_011507668.1:p.Thr970=
XM_011509367.1:c.2909C=	XP_011507669.1:p.Thr970=
XM_011509368.1:c.2327C=	XP_011507670.1:p.Thr776=
XM_011509369.1:c.1352C=	XP_011507671.1:p.Thr451=
XM_011509365.2:c.2909C=	XP_011507667.1:p.Thr970=
XM_011509369.2:c.1352C=	XP_011507671.1:p.Thr451=
XM_017000851.1:c.2066C=	XP_016856340.1:p.Thr689=
XM_017000852.1:c.3044C=	XP_016856341.1:p.Thr1015=
NM_201253.3:c.2909C= MANE Select	NP_957705.1:p.Thr970=
NM_001193640.2:c.2573C=	NP_001180569.1:p.Thr858=
NM_001257965.2:c.2837C=	NP_001244894.1:p.Thr946=
NR_047563.2:n.2862C=
NR_047564.2:n.3070C=
NM_001257966.2:c.2129-828C=	NP_001244895.1:n.2129-828C=