Canonical Allele Identifier: CA1884104348

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197833G= , CM000671.2:g.136197833G=	GRCh38
NC_000009.11:g.139089679G= , CM000671.1:g.139089679G=	GRCh37
NC_000009.10:g.138229500G=	NCBI36
NG_008097.1:g.12277C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371746.9:c.791-90C=	ENSP00000360811.3:n.791-90C=
ENST00000371748.10:c.776-90C= MANE Select	ENSP00000360813.4:n.776-90C=
ENST00000645419.1:n.1601-90C=
ENST00000371746.7:c.791-90C=	ENSP00000360811.3:n.791-90C=
ENST00000371748.9:c.776-90C=	ENSP00000360813.4:n.776-90C=
ENST00000619587.1:c.743-90C=	ENSP00000483080.1:n.743-90C=
NM_014564.3:c.791-90C=	NP_055379.1:n.791-90C=
NM_178138.4:c.776-90C=	NP_835258.1:n.776-90C=
XM_005263410.1:c.743-90C=	XP_005263467.1:n.743-90C=
NM_001363746.1:c.743-90C=	NP_001350675.1:n.743-90C=
NM_014564.4:c.791-90C=	NP_055379.1:n.791-90C=
NM_178138.5:c.776-90C=	NP_835258.1:n.776-90C=
XM_017015168.1:c.704-90C=	XP_016870657.1:n.704-90C=
NM_178138.6:c.776-90C= MANE Select	NP_835258.1:n.776-90C=
NM_014564.5:c.791-90C=	NP_055379.1:n.791-90C=