Canonical Allele Identifier: CA386860714
Gene: LHX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.113463332C>T , CM000674.2:g.113463332C>T GRCh38
NC_000012.11:g.113901137C>T , CM000674.1:g.113901137C>T GRCh37
NC_000012.10:g.112385520C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261731.4:c.1067G>A MANE Select ENSP00000261731.2:p.Gly356Asp
ENST00000261731.3:c.1067G>A ENSP00000261731.2:p.Gly356Asp
NM_022363.2:c.1067G>A NP_071758.1:p.Gly356Asp
NM_022363.3:c.1067G>A MANE Select NP_071758.1:p.Gly356Asp