Canonical Allele Identifier: CA3901135

Gene: LCA5

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.79513594T>C , CM000668.2:g.79513594T>C	GRCh38
NC_000006.11:g.80223311T>C , CM000668.1:g.80223311T>C	GRCh37
NC_000006.10:g.80280030T>C	NCBI36
NG_016011.1:g.28837A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001122769.3:c.338A>G MANE Select	NP_001116241.1:p.Asn113Ser
ENST00000369846.9:c.338A>G MANE Select	ENSP00000358861.4:p.Asn113Ser
NM_001122769.2:c.338A>G	NP_001116241.1:p.Asn113Ser
NM_181714.3:c.338A>G	NP_859065.2:p.Asn113Ser
NM_181714.4:c.338A>G	NP_859065.2:p.Asn113Ser
ENST00000369846.8:c.338A>G	ENSP00000358861.4:p.Asn113Ser
ENST00000392959.5:c.338A>G	ENSP00000376686.1:p.Asn113Ser
ENST00000467898.3:c.338A>G	ENSP00000474463.1:p.Asn113Ser
XM_005248665.3:c.338A>G	XP_005248722.1:p.Asn113Ser
XM_005248665.4:c.338A>G	XP_005248722.1:p.Asn113Ser
XM_011535504.1:c.338A>G	XP_011533806.1:p.Asn113Ser