Canonical Allele Identifier: CA1272104
Community Standard Title: NM_033343.4(LHX4):c.*17C>T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180274596C>T , CM000663.2:g.180274596C>T GRCh38
NC_000001.10:g.180243731C>T , CM000663.1:g.180243731C>T GRCh37
NC_000001.9:g.178510354C>T NCBI36
NG_008081.1:g.49290C>T

Transcript Alleles

HGVS Amino-acid Change
NM_033343.4:c.*17C>T (LHX4) MANE Select NP_203129.1:n.*17C>T
ENST00000263726.4:c.*17C>T (LHX4) MANE Select ENSP00000263726.2:n.*17C>T
NM_033343.3:c.*17C>T (LHX4) NP_203129.1:n.*17C>T
NR_037642.1:n.31+55G>A (LHX4-AS1)
ENST00000263726.3:c.*17C>T (LHX4) ENSP00000263726.2:n.*17C>T
ENST00000415414.5:n.31+55G>A (ACBD6)
ENST00000440959.2:n.1574+55G>A (ACBD6)
ENST00000622400.1:n.63+55G>A (ACBD6)
ENST00000642319.1:c.*936+55G>A (ACBD6) ENSP00000495710.1:n.*936+55G>A
ENST00000645415.1:c.*1169+55G>A (ACBD6) ENSP00000494507.1:n.*1169+55G>A
XM_011510105.1:c.*17C>T (LHX4) XP_011508407.1:n.*17C>T
XM_011510105.2:c.*17C>T (LHX4) XP_011508407.1:n.*17C>T
XM_011510106.1:c.*17C>T (LHX4) XP_011508408.1:n.*17C>T
XM_011510106.3:c.*17C>T (LHX4) XP_011508408.1:n.*17C>T
XM_011510107.1:c.*17C>T (LHX4) XP_011508409.1:n.*17C>T
XM_011510108.1:c.*17C>T (LHX4) XP_011508410.1:n.*17C>T
XM_011510108.2:c.*17C>T (LHX4) XP_011508410.1:n.*17C>T
XM_017002755.1:c.*17C>T (LHX4) XP_016858244.1:n.*17C>T
XR_001737484.2:n.2151G>A (ACBD6)
XR_001737485.2:n.2134G>A (ACBD6)
XR_002957801.1:n.2053G>A (ACBD6)
XR_921977.3:n.2278G>A (ACBD6)
XR_921978.3:n.2282G>A (ACBD6)