Canonical Allele Identifier: CA451117782
Community Standard Title: NM_001122769.3(LCA5):c.1545A>G (p.Ser515=)
Gene: LCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79487553T>C , CM000668.2:g.79487553T>C GRCh38
NC_000006.11:g.80197270T>C , CM000668.1:g.80197270T>C GRCh37
NC_000006.10:g.80253989T>C NCBI36
NG_016011.1:g.54878A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001122769.3:c.1545A>G MANE Select NP_001116241.1:p.Ser515=
ENST00000369846.9:c.1545A>G MANE Select ENSP00000358861.4:p.Ser515=
NM_001122769.2:c.1545A>G NP_001116241.1:p.Ser515=
NM_181714.3:c.1545A>G NP_859065.2:p.Ser515=
NM_181714.4:c.1545A>G NP_859065.2:p.Ser515=
ENST00000369846.8:c.1545A>G ENSP00000358861.4:p.Ser515=
ENST00000392959.5:c.1545A>G ENSP00000376686.1:p.Ser515=
XM_005248665.3:c.1545A>G XP_005248722.1:p.Ser515=
XM_005248665.4:c.1545A>G XP_005248722.1:p.Ser515=
XM_011535504.1:c.1545A>G XP_011533806.1:p.Ser515=
XR_001744213.1:n.2169-880T>C
XR_001744214.1:n.2131-880T>C
XR_942715.1:n.544-880T>C
XR_942716.1:n.506-880T>C
XR_942717.1:n.778-880T>C