Canonical Allele Identifier: CA250575
Gene: LHX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136200700T>A , CM000671.2:g.136200700T>A GRCh38
NC_000009.11:g.139092546T>A , CM000671.1:g.139092546T>A GRCh37
NC_000009.10:g.138232367T>A NCBI36
NG_008097.1:g.9410A>T

Transcript Alleles

HGVS Amino-acid Change
NM_178138.6:c.133A>T MANE Select NP_835258.1:p.Lys45Ter
ENST00000371748.10:c.133A>T MANE Select ENSP00000360813.4:p.Lys45Ter
NM_001363746.1:c.100A>T NP_001350675.1:p.Lys34Ter
NM_014564.3:c.148A>T NP_055379.1:p.Lys50Ter
NM_014564.4:c.148A>T NP_055379.1:p.Lys50Ter
NM_014564.5:c.148A>T NP_055379.1:p.Lys50Ter
NM_178138.4:c.133A>T NP_835258.1:p.Lys45Ter
NM_178138.5:c.133A>T NP_835258.1:p.Lys45Ter
ENST00000371746.7:c.148A>T ENSP00000360811.3:p.Lys50Ter
ENST00000371746.9:c.148A>T ENSP00000360811.3:p.Lys50Ter
ENST00000371748.9:c.133A>T ENSP00000360813.4:p.Lys45Ter
ENST00000619587.1:c.100A>T ENSP00000483080.1:p.Lys34Ter
ENST00000645419.1:n.257A>T
XM_005263410.1:c.100A>T XP_005263467.1:p.Lys34Ter
XM_017015168.1:c.61A>T XP_016870657.1:p.Lys21Ter