Canonical Allele Identifier: CA343595538
Gene: LHX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180266453A>C , CM000663.2:g.180266453A>C GRCh38
NC_000001.10:g.180235588A>C , CM000663.1:g.180235588A>C GRCh37
NC_000001.9:g.178502211A>C NCBI36
NG_008081.1:g.41147A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.310A>C MANE Select ENSP00000263726.2:p.Lys104Gln
ENST00000263726.3:c.310A>C ENSP00000263726.2:p.Lys104Gln
ENST00000561113.1:c.247A>C
NM_033343.3:c.310A>C NP_203129.1:p.Lys104Gln
XM_011510105.1:c.127A>C XP_011508407.1:p.Lys43Gln
XM_011510106.1:c.127A>C XP_011508408.1:p.Lys43Gln
XM_011510107.1:c.85A>C XP_011508409.1:p.Lys29Gln
XM_011510108.1:c.85A>C XP_011508410.1:p.Lys29Gln
XM_011510105.2:c.127A>C XP_011508407.1:p.Lys43Gln
XM_011510106.3:c.127A>C XP_011508408.1:p.Lys43Gln
XM_011510108.2:c.85A>C XP_011508410.1:p.Lys29Gln
XM_017002755.1:c.85A>C XP_016858244.1:p.Lys29Gln
NM_033343.4:c.310A>C MANE Select NP_203129.1:p.Lys104Gln