Canonical Allele Identifier: CA364643624
Gene: LCA5 HGNC NCBI

Linked Data

dbSNP Id: rs757095417
gnomAD v4: 6-79491592-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79491592G>C , CM000668.2:g.79491592G>C GRCh38
NC_000006.11:g.80201309G>C , CM000668.1:g.80201309G>C GRCh37
NC_000006.10:g.80258028G>C NCBI36
NG_016011.1:g.50839C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369846.9:c.1094C>G MANE Select ENSP00000358861.4:p.Thr365Ser
ENST00000369846.8:c.1094C>G ENSP00000358861.4:p.Thr365Ser
ENST00000392959.5:c.1094C>G ENSP00000376686.1:p.Thr365Ser
ENST00000467898.3:c.1094C>G ENSP00000474463.1:p.Thr365Ser
NM_001122769.2:c.1094C>G NP_001116241.1:p.Thr365Ser
NM_181714.3:c.1094C>G NP_859065.2:p.Thr365Ser
XM_005248665.3:c.1094C>G XP_005248722.1:p.Thr365Ser
XM_011535504.1:c.1094C>G XP_011533806.1:p.Thr365Ser
XM_005248665.4:c.1094C>G XP_005248722.1:p.Thr365Ser
NM_001122769.3:c.1094C>G MANE Select NP_001116241.1:p.Thr365Ser
NM_181714.4:c.1094C>G NP_859065.2:p.Thr365Ser