Canonical Allele Identifier: CA1272077

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180274459G>A , CM000663.2:g.180274459G>A GRCh38
NC_000001.10:g.180243594G>A , CM000663.1:g.180243594G>A GRCh37
NC_000001.9:g.178510217G>A NCBI36
NG_008081.1:g.49153G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.1053G>A (LHX4) MANE Select ENSP00000263726.2:p.Thr351=
ENST00000642319.1:c.*936+192C>T (ACBD6) ENSP00000495710.1:n.*936+192C>T
ENST00000645415.1:c.*1169+192C>T (ACBD6) ENSP00000494507.1:n.*1169+192C>T
ENST00000263726.3:c.1053G>A (LHX4) ENSP00000263726.2:p.Thr351=
ENST00000415414.5:n.31+192C>T (ACBD6)
ENST00000440959.2:n.1574+192C>T (ACBD6)
ENST00000622400.1:n.63+192C>T (ACBD6)
NM_033343.3:c.1053G>A (LHX4) NP_203129.1:p.Thr351=
NR_037642.1:n.31+192C>T (LHX4-AS1)
XM_011510105.1:c.870G>A (LHX4) XP_011508407.1:p.Thr290=
XM_011510106.1:c.870G>A (LHX4) XP_011508408.1:p.Thr290=
XM_011510107.1:c.828G>A (LHX4) XP_011508409.1:p.Thr276=
XM_011510108.1:c.828G>A (LHX4) XP_011508410.1:p.Thr276=
XM_011510105.2:c.870G>A (LHX4) XP_011508407.1:p.Thr290=
XM_011510106.3:c.870G>A (LHX4) XP_011508408.1:p.Thr290=
XM_011510108.2:c.828G>A (LHX4) XP_011508410.1:p.Thr276=
XM_017002755.1:c.828G>A (LHX4) XP_016858244.1:p.Thr276=
XR_001737484.2:n.2288C>T (ACBD6)
XR_001737485.2:n.2271C>T (ACBD6)
XR_002957801.1:n.2190C>T (ACBD6)
XR_921977.3:n.2415C>T (ACBD6)
XR_921978.3:n.2419C>T (ACBD6)
NM_033343.4:c.1053G>A (LHX4) MANE Select NP_203129.1:p.Thr351=