Canonical Allele Identifier: CA2649358802

Gene: LHX4

Linked Data

• gnomAD v4: 1-180266301-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266301G>A , CM000663.2:g.180266301G>A	GRCh38
NC_000001.10:g.180235436G>A , CM000663.1:g.180235436G>A	GRCh37
NC_000001.9:g.178502059G>A	NCBI36
NG_008081.1:g.40995G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263726.4:c.249-91G>A MANE Select	ENSP00000263726.2:n.249-91G>A
ENST00000263726.3:c.249-91G>A	ENSP00000263726.2:n.249-91G>A
ENST00000561113.1:c.186-91G>A
NM_033343.3:c.249-91G>A	NP_203129.1:n.249-91G>A
XM_011510105.1:c.66-91G>A	XP_011508407.1:n.66-91G>A
XM_011510106.1:c.66-91G>A	XP_011508408.1:n.66-91G>A
XM_011510107.1:c.23+48G>A	XP_011508409.1:n.23+48G>A
XM_011510108.1:c.23+48G>A	XP_011508410.1:n.23+48G>A
XM_011510105.2:c.66-91G>A	XP_011508407.1:n.66-91G>A
XM_011510106.3:c.66-91G>A	XP_011508408.1:n.66-91G>A
XM_011510108.2:c.23+48G>A	XP_011508410.1:n.23+48G>A
XM_017002755.1:c.23+48G>A	XP_016858244.1:n.23+48G>A
NM_033343.4:c.249-91G>A MANE Select	NP_203129.1:n.249-91G>A