Canonical Allele Identifier: CA1640630142

Gene: LCA5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79493647T= , CM000668.2:g.79493647T=	GRCh38
NC_000006.11:g.80203364T= , CM000668.1:g.80203364T=	GRCh37
NC_000006.10:g.80260083T=	NCBI36
NG_016011.1:g.48784A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000369846.9:c.824A= MANE Select	ENSP00000358861.4:p.Gln275=
ENST00000369846.8:c.824A=	ENSP00000358861.4:p.Gln275=
ENST00000392959.5:c.824A=	ENSP00000376686.1:p.Gln275=
ENST00000467898.3:c.824A=	ENSP00000474463.1:p.Gln275=
NM_001122769.2:c.824A=	NP_001116241.1:p.Gln275=
NM_181714.3:c.824A=	NP_859065.2:p.Gln275=
XM_005248665.3:c.824A=	XP_005248722.1:p.Gln275=
XM_011535504.1:c.824A=	XP_011533806.1:p.Gln275=
XM_005248665.4:c.824A=	XP_005248722.1:p.Gln275=
NM_001122769.3:c.824A= MANE Select	NP_001116241.1:p.Gln275=
NM_181714.4:c.824A=	NP_859065.2:p.Gln275=