Canonical Allele Identifier: CA343595562

Gene: LHX4

Linked Data

• MyVariant Identifiers: chr1:g.180235594C>T (hg19) ; chr1:g.180266459C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266459C>T , CM000663.2:g.180266459C>T	GRCh38
NC_000001.10:g.180235594C>T , CM000663.1:g.180235594C>T	GRCh37
NC_000001.9:g.178502217C>T	NCBI36
NG_008081.1:g.41153C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.316C>T MANE Select	ENSP00000263726.2:p.Gln106Ter
ENST00000263726.3:c.316C>T	ENSP00000263726.2:p.Gln106Ter
ENST00000561113.1:c.253C>T
NM_033343.3:c.316C>T	NP_203129.1:p.Gln106Ter
XM_011510105.1:c.133C>T	XP_011508407.1:p.Gln45Ter
XM_011510106.1:c.133C>T	XP_011508408.1:p.Gln45Ter
XM_011510107.1:c.91C>T	XP_011508409.1:p.Gln31Ter
XM_011510108.1:c.91C>T	XP_011508410.1:p.Gln31Ter
XM_011510105.2:c.133C>T	XP_011508407.1:p.Gln45Ter
XM_011510106.3:c.133C>T	XP_011508408.1:p.Gln45Ter
XM_011510108.2:c.91C>T	XP_011508410.1:p.Gln31Ter
XM_017002755.1:c.91C>T	XP_016858244.1:p.Gln31Ter
NM_033343.4:c.316C>T MANE Select	NP_203129.1:p.Gln106Ter