Canonical Allele Identifier: CA364629426
Community Standard Title: NM_001122769.3(LCA5):c.346C>T (p.Gln116Ter)
Gene: LCA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79513586G>A , CM000668.2:g.79513586G>A GRCh38
NC_000006.11:g.80223303G>A , CM000668.1:g.80223303G>A GRCh37
NC_000006.10:g.80280022G>A NCBI36
NG_016011.1:g.28845C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001122769.3:c.346C>T MANE Select NP_001116241.1:p.Gln116Ter
ENST00000369846.9:c.346C>T MANE Select ENSP00000358861.4:p.Gln116Ter
NM_001122769.2:c.346C>T NP_001116241.1:p.Gln116Ter
NM_181714.3:c.346C>T NP_859065.2:p.Gln116Ter
NM_181714.4:c.346C>T NP_859065.2:p.Gln116Ter
ENST00000369846.8:c.346C>T ENSP00000358861.4:p.Gln116Ter
ENST00000392959.5:c.346C>T ENSP00000376686.1:p.Gln116Ter
ENST00000467898.3:c.346C>T ENSP00000474463.1:p.Gln116Ter
XM_005248665.3:c.346C>T XP_005248722.1:p.Gln116Ter
XM_005248665.4:c.346C>T XP_005248722.1:p.Gln116Ter
XM_011535504.1:c.346C>T XP_011533806.1:p.Gln116Ter