Canonical Allele Identifier: CA1210607039
Gene: LHX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180266317G= , CM000663.2:g.180266317G= GRCh38
NC_000001.10:g.180235452G= , CM000663.1:g.180235452G= GRCh37
NC_000001.9:g.178502075G= NCBI36
NG_008081.1:g.41011G=

Transcript Alleles

HGVS Amino-acid change
ENST00000263726.4:c.249-75G= MANE Select ENSP00000263726.2:n.249-75G=
ENST00000263726.3:c.249-75G= ENSP00000263726.2:n.249-75G=
ENST00000561113.1:c.186-75G=
NM_033343.3:c.249-75G= NP_203129.1:n.249-75G=
XM_011510105.1:c.66-75G= XP_011508407.1:n.66-75G=
XM_011510106.1:c.66-75G= XP_011508408.1:n.66-75G=
XM_011510107.1:c.23+64G= XP_011508409.1:n.23+64G=
XM_011510108.1:c.23+64G= XP_011508410.1:n.23+64G=
XM_011510105.2:c.66-75G= XP_011508407.1:n.66-75G=
XM_011510106.3:c.66-75G= XP_011508408.1:n.66-75G=
XM_011510108.2:c.23+64G= XP_011508410.1:n.23+64G=
XM_017002755.1:c.23+64G= XP_016858244.1:n.23+64G=
NM_033343.4:c.249-75G= MANE Select NP_203129.1:n.249-75G=