Canonical Allele Identifier: CA343595743
Gene: LHX4 HGNC NCBI

Linked Data

dbSNP Id: rs1286712820

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.180266506C>A , CM000663.2:g.180266506C>A GRCh38
NC_000001.10:g.180235641C>A , CM000663.1:g.180235641C>A GRCh37
NC_000001.9:g.178502264C>A NCBI36
NG_008081.1:g.41200C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263726.4:c.363C>A MANE Select ENSP00000263726.2:p.Asn121Lys
ENST00000263726.3:c.363C>A ENSP00000263726.2:p.Asn121Lys
ENST00000561113.1:c.300C>A
NM_033343.3:c.363C>A NP_203129.1:p.Asn121Lys
XM_011510105.1:c.180C>A XP_011508407.1:p.Asn60Lys
XM_011510106.1:c.180C>A XP_011508408.1:p.Asn60Lys
XM_011510107.1:c.138C>A XP_011508409.1:p.Asn46Lys
XM_011510108.1:c.138C>A XP_011508410.1:p.Asn46Lys
XM_011510105.2:c.180C>A XP_011508407.1:p.Asn60Lys
XM_011510106.3:c.180C>A XP_011508408.1:p.Asn60Lys
XM_011510108.2:c.138C>A XP_011508410.1:p.Asn46Lys
XM_017002755.1:c.138C>A XP_016858244.1:p.Asn46Lys
NM_033343.4:c.363C>A MANE Select NP_203129.1:p.Asn121Lys