Canonical Allele Identifier: CA1218063043

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421204A= , CM000663.2:g.197421204A=	GRCh38
NC_000001.10:g.197390334A= , CM000663.1:g.197390334A=	GRCh37
NC_000001.9:g.195656957A=	NCBI36
NG_008483.1:g.157927A=
NG_008483.2:g.224743A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1376A= MANE Select	ENSP00000356370.3:p.His459=
ENST00000638467.1:c.1376A=	ENSP00000491102.1:p.His459=
ENST00000681519.1:c.257A=	ENSP00000505267.1:p.His86=
ENST00000367397.1:c.-482A=	ENSP00000356367.1:n.-482A=
ENST00000367399.6:c.1040A=	ENSP00000356369.2:p.His347=
ENST00000367400.7:c.1376A=	ENSP00000356370.3:p.His459=
ENST00000476483.1:n.336A=
ENST00000484075.5:c.1376A=	ENSP00000433932.1:p.His459=
ENST00000535699.5:c.1169A=	ENSP00000438786.1:p.His390=
ENST00000538660.5:c.1376A=	ENSP00000438091.1:p.His459=
NM_001193640.1:c.1040A=	NP_001180569.1:p.His347=
NM_001257965.1:c.1169A=	NP_001244894.1:p.His390=
NM_001257966.1:c.1376A=	NP_001244895.1:p.His459=
NM_201253.2:c.1376A=	NP_957705.1:p.His459=
NR_047563.1:n.1585A=
NR_047564.1:n.1585A=
XM_011509365.1:c.1376A=	XP_011507667.1:p.His459=
XM_011509366.1:c.1376A=	XP_011507668.1:p.His459=
XM_011509367.1:c.1376A=	XP_011507669.1:p.His459=
XM_011509368.1:c.794A=	XP_011507670.1:p.His265=
XM_011509369.1:c.-182A=	XP_011507671.1:n.-182A=
XM_011509365.2:c.1376A=	XP_011507667.1:p.His459=
XM_011509369.2:c.-182A=	XP_011507671.1:n.-182A=
XM_017000851.1:c.533A=	XP_016856340.1:p.His178=
XM_017000852.1:c.1376A=	XP_016856341.1:p.His459=
NM_201253.3:c.1376A= MANE Select	NP_957705.1:p.His459=
NM_001193640.2:c.1040A=	NP_001180569.1:p.His347=
NM_001257965.2:c.1169A=	NP_001244894.1:p.His390=
NR_047563.2:n.1537A=
NR_047564.2:n.1537A=
NM_001257966.2:c.1376A=	NP_001244895.1:p.His459=