Canonical Allele Identifier: CA1884103929
Gene: LHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136197659G= , CM000671.2:g.136197659G= GRCh38
NC_000009.11:g.139089505G= , CM000671.1:g.139089505G= GRCh37
NC_000009.10:g.138229326G= NCBI36
NG_008097.1:g.12451C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371746.9:c.875C= ENSP00000360811.3:p.Ser292=
ENST00000371748.10:c.860C= MANE Select ENSP00000360813.4:p.Ser287=
ENST00000645419.1:n.1685C=
ENST00000371746.7:c.875C= ENSP00000360811.3:p.Ser292=
ENST00000371748.9:c.860C= ENSP00000360813.4:p.Ser287=
ENST00000619587.1:c.827C= ENSP00000483080.1:p.Ser276=
NM_014564.3:c.875C= NP_055379.1:p.Ser292=
NM_178138.4:c.860C= NP_835258.1:p.Ser287=
XM_005263410.1:c.827C= XP_005263467.1:p.Ser276=
NM_001363746.1:c.827C= NP_001350675.1:p.Ser276=
NM_014564.4:c.875C= NP_055379.1:p.Ser292=
NM_178138.5:c.860C= NP_835258.1:p.Ser287=
XM_017015168.1:c.788C= XP_016870657.1:p.Ser263=
NM_178138.6:c.860C= MANE Select NP_835258.1:p.Ser287=
NM_014564.5:c.875C= NP_055379.1:p.Ser292=