Canonical Allele Identifier: CA1884103647
Gene: LHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136197560G= , CM000671.2:g.136197560G= GRCh38
NC_000009.11:g.139089406G= , CM000671.1:g.139089406G= GRCh37
NC_000009.10:g.138229227G= NCBI36
NG_008097.1:g.12550C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371746.9:c.974C= ENSP00000360811.3:p.Ser325=
ENST00000371748.10:c.959C= MANE Select ENSP00000360813.4:p.Ser320=
ENST00000645419.1:n.1784C=
ENST00000371746.7:c.974C= ENSP00000360811.3:p.Ser325=
ENST00000371748.9:c.959C= ENSP00000360813.4:p.Ser320=
ENST00000619587.1:c.926C= ENSP00000483080.1:p.Ser309=
NM_014564.3:c.974C= NP_055379.1:p.Ser325=
NM_178138.4:c.959C= NP_835258.1:p.Ser320=
XM_005263410.1:c.926C= XP_005263467.1:p.Ser309=
NM_001363746.1:c.926C= NP_001350675.1:p.Ser309=
NM_014564.4:c.974C= NP_055379.1:p.Ser325=
NM_178138.5:c.959C= NP_835258.1:p.Ser320=
XM_017015168.1:c.887C= XP_016870657.1:p.Ser296=
NM_178138.6:c.959C= MANE Select NP_835258.1:p.Ser320=
NM_014564.5:c.974C= NP_055379.1:p.Ser325=