Canonical Allele Identifier: CA343595541
Gene: LHX4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.310A>T MANE Select ENSP00000263726.2:p.Lys104Ter
ENST00000263726.3:c.310A>T ENSP00000263726.2:p.Lys104Ter
ENST00000561113.1:c.247A>T
NM_033343.3:c.310A>T NP_203129.1:p.Lys104Ter
XM_011510105.1:c.127A>T XP_011508407.1:p.Lys43Ter
XM_011510106.1:c.127A>T XP_011508408.1:p.Lys43Ter
XM_011510107.1:c.85A>T XP_011508409.1:p.Lys29Ter
XM_011510108.1:c.85A>T XP_011508410.1:p.Lys29Ter
XM_011510105.2:c.127A>T XP_011508407.1:p.Lys43Ter
XM_011510106.3:c.127A>T XP_011508408.1:p.Lys43Ter
XM_011510108.2:c.85A>T XP_011508410.1:p.Lys29Ter
XM_017002755.1:c.85A>T XP_016858244.1:p.Lys29Ter
NM_033343.4:c.310A>T MANE Select NP_203129.1:p.Lys104Ter