Canonical Allele Identifier: CA451009927
Gene: LCA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.80201389G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.79491672G>A , CM000668.2:g.79491672G>A GRCh38
NC_000006.11:g.80201389G>A , CM000668.1:g.80201389G>A GRCh37
NC_000006.10:g.80258108G>A NCBI36
NG_016011.1:g.50759C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369846.9:c.1014C>T MANE Select ENSP00000358861.4:p.Asp338=
ENST00000369846.8:c.1014C>T ENSP00000358861.4:p.Asp338=
ENST00000392959.5:c.1014C>T ENSP00000376686.1:p.Asp338=
ENST00000467898.3:c.1014C>T ENSP00000474463.1:p.Asp338=
NM_001122769.2:c.1014C>T NP_001116241.1:p.Asp338=
NM_181714.3:c.1014C>T NP_859065.2:p.Asp338=
XM_005248665.3:c.1014C>T XP_005248722.1:p.Asp338=
XM_011535504.1:c.1014C>T XP_011533806.1:p.Asp338=
XM_005248665.4:c.1014C>T XP_005248722.1:p.Asp338=
NM_001122769.3:c.1014C>T MANE Select NP_001116241.1:p.Asp338=
NM_181714.4:c.1014C>T NP_859065.2:p.Asp338=