Canonical Allele Identifier: CA375518781

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197555-C-G
• MyVariant Identifiers: chr9:g.139089401C>G (hg19) ; chr9:g.136197555C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197555C>G , CM000671.2:g.136197555C>G	GRCh38
NC_000009.11:g.139089401C>G , CM000671.1:g.139089401C>G	GRCh37
NC_000009.10:g.138229222C>G	NCBI36
NG_008097.1:g.12555G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.979G>C	ENSP00000360811.3:p.Ala327Pro
ENST00000371748.10:c.964G>C MANE Select	ENSP00000360813.4:p.Ala322Pro
ENST00000645419.1:n.1789G>C
ENST00000371746.7:c.979G>C	ENSP00000360811.3:p.Ala327Pro
ENST00000371748.9:c.964G>C	ENSP00000360813.4:p.Ala322Pro
ENST00000619587.1:c.931G>C	ENSP00000483080.1:p.Ala311Pro
NM_014564.3:c.979G>C	NP_055379.1:p.Ala327Pro
NM_178138.4:c.964G>C	NP_835258.1:p.Ala322Pro
XM_005263410.1:c.931G>C	XP_005263467.1:p.Ala311Pro
NM_001363746.1:c.931G>C	NP_001350675.1:p.Ala311Pro
NM_014564.4:c.979G>C	NP_055379.1:p.Ala327Pro
NM_178138.5:c.964G>C	NP_835258.1:p.Ala322Pro
XM_017015168.1:c.892G>C	XP_016870657.1:p.Ala298Pro
NM_178138.6:c.964G>C MANE Select	NP_835258.1:p.Ala322Pro
NM_014564.5:c.979G>C	NP_055379.1:p.Ala327Pro