Canonical Allele Identifier: CA1218063245

Gene: CRB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197421714A= , CM000663.2:g.197421714A=	GRCh38
NC_000001.10:g.197390844A= , CM000663.1:g.197390844A=	GRCh37
NC_000001.9:g.195657467A=	NCBI36
NG_008483.1:g.158437A=
NG_008483.2:g.225253A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367400.8:c.1886A= MANE Select	ENSP00000356370.3:p.Asn629=
ENST00000638467.1:c.1886A=	ENSP00000491102.1:p.Asn629=
ENST00000681519.1:c.767A=	ENSP00000505267.1:p.Asn256=
ENST00000367397.1:c.29A=	ENSP00000356367.1:p.Asn10=
ENST00000367399.6:c.1550A=	ENSP00000356369.2:p.Asn517=
ENST00000367400.7:c.1886A=	ENSP00000356370.3:p.Asn629=
ENST00000484075.5:c.1886A=	ENSP00000433932.1:p.Asn629=
ENST00000535699.5:c.1679A=	ENSP00000438786.1:p.Asn560=
ENST00000538660.5:c.1886A=	ENSP00000438091.1:p.Asn629=
NM_001193640.1:c.1550A=	NP_001180569.1:p.Asn517=
NM_001257965.1:c.1679A=	NP_001244894.1:p.Asn560=
NM_001257966.1:c.1886A=	NP_001244895.1:p.Asn629=
NM_201253.2:c.1886A=	NP_957705.1:p.Asn629=
NR_047563.1:n.1923-36A=
NR_047564.1:n.2095A=
XM_011509365.1:c.1886A=	XP_011507667.1:p.Asn629=
XM_011509366.1:c.1886A=	XP_011507668.1:p.Asn629=
XM_011509367.1:c.1886A=	XP_011507669.1:p.Asn629=
XM_011509368.1:c.1304A=	XP_011507670.1:p.Asn435=
XM_011509369.1:c.329A=	XP_011507671.1:p.Asn110=
XM_011509365.2:c.1886A=	XP_011507667.1:p.Asn629=
XM_011509369.2:c.329A=	XP_011507671.1:p.Asn110=
XM_017000851.1:c.1043A=	XP_016856340.1:p.Asn348=
XM_017000852.1:c.1886A=	XP_016856341.1:p.Asn629=
NM_201253.3:c.1886A= MANE Select	NP_957705.1:p.Asn629=
NM_001193640.2:c.1550A=	NP_001180569.1:p.Asn517=
NM_001257965.2:c.1679A=	NP_001244894.1:p.Asn560=
NR_047563.2:n.1875-36A=
NR_047564.2:n.2047A=
NM_001257966.2:c.1886A=	NP_001244895.1:p.Asn629=