Canonical Allele Identifier: CA343595571
Gene: LHX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180266462G>A , CM000663.2:g.180266462G>A GRCh38
NC_000001.10:g.180235597G>A , CM000663.1:g.180235597G>A GRCh37
NC_000001.9:g.178502220G>A NCBI36
NG_008081.1:g.41156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.319G>A MANE Select ENSP00000263726.2:p.Asp107Asn
ENST00000263726.3:c.319G>A ENSP00000263726.2:p.Asp107Asn
ENST00000561113.1:c.256G>A
NM_033343.3:c.319G>A NP_203129.1:p.Asp107Asn
XM_011510105.1:c.136G>A XP_011508407.1:p.Asp46Asn
XM_011510106.1:c.136G>A XP_011508408.1:p.Asp46Asn
XM_011510107.1:c.94G>A XP_011508409.1:p.Asp32Asn
XM_011510108.1:c.94G>A XP_011508410.1:p.Asp32Asn
XM_011510105.2:c.136G>A XP_011508407.1:p.Asp46Asn
XM_011510106.3:c.136G>A XP_011508408.1:p.Asp46Asn
XM_011510108.2:c.94G>A XP_011508410.1:p.Asp32Asn
XM_017002755.1:c.94G>A XP_016858244.1:p.Asp32Asn
NM_033343.4:c.319G>A MANE Select NP_203129.1:p.Asp107Asn