Canonical Allele Identifier: CA1271826
Community Standard Title: NM_033343.4(LHX4):c.248+13G>A
Gene: LHX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180248469G>A , CM000663.2:g.180248469G>A GRCh38
NC_000001.10:g.180217604G>A , CM000663.1:g.180217604G>A GRCh37
NC_000001.9:g.178484227G>A NCBI36
NG_008081.1:g.23163G>A

Transcript Alleles

HGVS Amino-acid Change
NM_033343.4:c.248+13G>A MANE Select NP_203129.1:n.248+13G>A
ENST00000263726.4:c.248+13G>A MANE Select ENSP00000263726.2:n.248+13G>A
NM_033343.3:c.248+13G>A NP_203129.1:n.248+13G>A
ENST00000263726.3:c.248+13G>A ENSP00000263726.2:n.248+13G>A
ENST00000558139.1:n.493G>A
ENST00000561113.1:c.185G>A
XM_011510105.1:c.65+13G>A XP_011508407.1:n.65+13G>A
XM_011510105.2:c.65+13G>A XP_011508407.1:n.65+13G>A
XM_011510106.1:c.65+13G>A XP_011508408.1:n.65+13G>A
XM_011510106.3:c.65+13G>A XP_011508408.1:n.65+13G>A
XM_011510108.1:c.-29+13G>A XP_011508410.1:n.-29+13G>A
XM_011510108.2:c.-29+13G>A XP_011508410.1:n.-29+13G>A