Canonical Allele Identifier: CA375518968

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197653-G-A
• MyVariant Identifiers: chr9:g.139089499G>A (hg19) ; chr9:g.136197653G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197653G>A , CM000671.2:g.136197653G>A	GRCh38
NC_000009.11:g.139089499G>A , CM000671.1:g.139089499G>A	GRCh37
NC_000009.10:g.138229320G>A	NCBI36
NG_008097.1:g.12457C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.881C>T	ENSP00000360811.3:p.Ala294Val
ENST00000371748.10:c.866C>T MANE Select	ENSP00000360813.4:p.Ala289Val
ENST00000645419.1:n.1691C>T
ENST00000371746.7:c.881C>T	ENSP00000360811.3:p.Ala294Val
ENST00000371748.9:c.866C>T	ENSP00000360813.4:p.Ala289Val
ENST00000619587.1:c.833C>T	ENSP00000483080.1:p.Ala278Val
NM_014564.3:c.881C>T	NP_055379.1:p.Ala294Val
NM_178138.4:c.866C>T	NP_835258.1:p.Ala289Val
XM_005263410.1:c.833C>T	XP_005263467.1:p.Ala278Val
NM_001363746.1:c.833C>T	NP_001350675.1:p.Ala278Val
NM_014564.4:c.881C>T	NP_055379.1:p.Ala294Val
NM_178138.5:c.866C>T	NP_835258.1:p.Ala289Val
XM_017015168.1:c.794C>T	XP_016870657.1:p.Ala265Val
NM_178138.6:c.866C>T MANE Select	NP_835258.1:p.Ala289Val
NM_014564.5:c.881C>T	NP_055379.1:p.Ala294Val