Canonical Allele Identifier: CA1271979

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180271932G>A , CM000663.2:g.180271932G>A GRCh38
NC_000001.10:g.180241067G>A , CM000663.1:g.180241067G>A GRCh37
NC_000001.9:g.178507690G>A NCBI36
NG_008081.1:g.46626G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.704G>A (LHX4) MANE Select ENSP00000263726.2:p.Arg235Gln
ENST00000642319.1:c.*1293C>T (ACBD6) ENSP00000495710.1:n.*1293C>T
ENST00000645415.1:c.*1526C>T (ACBD6) ENSP00000494507.1:n.*1526C>T
ENST00000263726.3:c.704G>A (LHX4) ENSP00000263726.2:p.Arg235Gln
ENST00000415414.5:n.388C>T (ACBD6)
NM_033343.3:c.704G>A (LHX4) NP_203129.1:p.Arg235Gln
NR_037642.1:n.388C>T (LHX4-AS1)
XM_011510105.1:c.521G>A (LHX4) XP_011508407.1:p.Arg174Gln
XM_011510106.1:c.521G>A (LHX4) XP_011508408.1:p.Arg174Gln
XM_011510107.1:c.479G>A (LHX4) XP_011508409.1:p.Arg160Gln
XM_011510108.1:c.479G>A (LHX4) XP_011508410.1:p.Arg160Gln
XM_011510105.2:c.521G>A (LHX4) XP_011508407.1:p.Arg174Gln
XM_011510106.3:c.521G>A (LHX4) XP_011508408.1:p.Arg174Gln
XM_011510108.2:c.479G>A (LHX4) XP_011508410.1:p.Arg160Gln
XM_017002755.1:c.479G>A (LHX4) XP_016858244.1:p.Arg160Gln
XR_001737484.2:n.4815C>T (ACBD6)
XR_001737485.2:n.4798C>T (ACBD6)
XR_002957801.1:n.4717C>T (ACBD6)
XR_921977.3:n.4942C>T (ACBD6)
XR_921978.3:n.4946C>T (ACBD6)
NM_033343.4:c.704G>A (LHX4) MANE Select NP_203129.1:p.Arg235Gln