Canonical Allele Identifier: CA364642803
Community Standard Title: NM_001122769.3(LCA5):c.1099-1G>A
Gene: LCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79489217C>T , CM000668.2:g.79489217C>T GRCh38
NC_000006.11:g.80198934C>T , CM000668.1:g.80198934C>T GRCh37
NC_000006.10:g.80255653C>T NCBI36
NG_016011.1:g.53214G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001122769.3:c.1099-1G>A MANE Select NP_001116241.1:n.1099-1G>A
ENST00000369846.9:c.1099-1G>A MANE Select ENSP00000358861.4:n.1099-1G>A
NM_001122769.2:c.1099-1G>A NP_001116241.1:n.1099-1G>A
NM_181714.3:c.1099-1G>A NP_859065.2:n.1099-1G>A
NM_181714.4:c.1099-1G>A NP_859065.2:n.1099-1G>A
ENST00000369846.8:c.1099-1G>A ENSP00000358861.4:n.1099-1G>A
ENST00000392959.5:c.1099-1G>A ENSP00000376686.1:n.1099-1G>A
ENST00000467898.3:c.1099-1G>A ENSP00000474463.1:n.1099-1G>A
XM_005248665.3:c.1099-1G>A XP_005248722.1:n.1099-1G>A
XM_005248665.4:c.1099-1G>A XP_005248722.1:n.1099-1G>A
XM_011535504.1:c.1099-1G>A XP_011533806.1:n.1099-1G>A
XR_001744213.1:n.2953C>T
XR_001744214.1:n.2915C>T