Canonical Allele Identifier: CA1884103913
Gene: LHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136197649C= , CM000671.2:g.136197649C= GRCh38
NC_000009.11:g.139089495C= , CM000671.1:g.139089495C= GRCh37
NC_000009.10:g.138229316C= NCBI36
NG_008097.1:g.12461G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371746.9:c.885G= ENSP00000360811.3:p.Leu295=
ENST00000371748.10:c.870G= MANE Select ENSP00000360813.4:p.Leu290=
ENST00000645419.1:n.1695G=
ENST00000371746.7:c.885G= ENSP00000360811.3:p.Leu295=
ENST00000371748.9:c.870G= ENSP00000360813.4:p.Leu290=
ENST00000619587.1:c.837G= ENSP00000483080.1:p.Leu279=
NM_014564.3:c.885G= NP_055379.1:p.Leu295=
NM_178138.4:c.870G= NP_835258.1:p.Leu290=
XM_005263410.1:c.837G= XP_005263467.1:p.Leu279=
NM_001363746.1:c.837G= NP_001350675.1:p.Leu279=
NM_014564.4:c.885G= NP_055379.1:p.Leu295=
NM_178138.5:c.870G= NP_835258.1:p.Leu290=
XM_017015168.1:c.798G= XP_016870657.1:p.Leu266=
NM_178138.6:c.870G= MANE Select NP_835258.1:p.Leu290=
NM_014564.5:c.885G= NP_055379.1:p.Leu295=