Canonical Allele Identifier: CA364629197
Community Standard Title: NM_001122769.3(LCA5):c.395A>G (p.Glu132Gly)
Gene: LCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79513537T>C , CM000668.2:g.79513537T>C GRCh38
NC_000006.11:g.80223254T>C , CM000668.1:g.80223254T>C GRCh37
NC_000006.10:g.80279973T>C NCBI36
NG_016011.1:g.28894A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001122769.3:c.395A>G MANE Select NP_001116241.1:p.Glu132Gly
ENST00000369846.9:c.395A>G MANE Select ENSP00000358861.4:p.Glu132Gly
NM_001122769.2:c.395A>G NP_001116241.1:p.Glu132Gly
NM_181714.3:c.395A>G NP_859065.2:p.Glu132Gly
NM_181714.4:c.395A>G NP_859065.2:p.Glu132Gly
ENST00000369846.8:c.395A>G ENSP00000358861.4:p.Glu132Gly
ENST00000392959.5:c.395A>G ENSP00000376686.1:p.Glu132Gly
ENST00000467898.3:c.395A>G ENSP00000474463.1:p.Glu132Gly
XM_005248665.3:c.395A>G XP_005248722.1:p.Glu132Gly
XM_005248665.4:c.395A>G XP_005248722.1:p.Glu132Gly
XM_011535504.1:c.395A>G XP_011533806.1:p.Glu132Gly