Canonical Allele Identifier: CA15114935
Gene: LHX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180248001G>A , CM000663.2:g.180248001G>A GRCh38
NC_000001.10:g.180217136G>A , CM000663.1:g.180217136G>A GRCh37
NC_000001.9:g.178483759G>A NCBI36
NG_008081.1:g.22695G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.77-284G>A MANE Select ENSP00000263726.2:n.77-284G>A
ENST00000263726.3:c.77-284G>A ENSP00000263726.2:n.77-284G>A
ENST00000558139.1:n.309-284G>A
NM_033343.3:c.77-284G>A NP_203129.1:n.77-284G>A
XM_011510105.1:c.-107-284G>A XP_011508407.1:n.-107-284G>A
XM_011510106.1:c.-107-284G>A XP_011508408.1:n.-107-284G>A
XM_011510105.2:c.-107-284G>A XP_011508407.1:n.-107-284G>A
XM_011510106.3:c.-107-284G>A XP_011508408.1:n.-107-284G>A
NM_033343.4:c.77-284G>A MANE Select NP_203129.1:n.77-284G>A