Canonical Allele Identifier: CA1140092503

Gene: LGR6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202218048G= , CM000663.2:g.202218048G=	GRCh38
NC_000001.10:g.202187176G= , CM000663.1:g.202187176G=	GRCh37
NC_000001.9:g.200453799G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367278.8:c.213-7375G= MANE Select	ENSP00000356247.3:n.213-7375G=
ENST00000255432.11:c.57-7375G=	ENSP00000255432.7:n.57-7375G=
ENST00000367278.7:c.213-7375G=	ENSP00000356247.3:n.213-7375G=
ENST00000423542.5:c.-11+7257G=	ENSP00000402284.1:n.-11+7257G=
ENST00000439764.2:c.83+3811G=	ENSP00000387869.2:n.83+3811G=
ENST00000487787.5:c.57-7375G=	ENSP00000422143.1:n.57-7375G=
NM_001017403.1:c.213-7375G=	NP_001017403.1:n.213-7375G=
NM_001017404.1:c.83+3811G=	NP_001017404.1:n.83+3811G=
NM_021636.2:c.57-7375G=	NP_067649.2:n.57-7375G=
XM_005245404.2:c.83+3811G=	XP_005245461.1:n.83+3811G=
XM_011509838.1:c.83+3811G=	XP_011508140.1:n.83+3811G=
XM_011509839.1:c.83+3811G=	XP_011508141.1:n.83+3811G=
XM_011509840.1:c.83+3811G=	XP_011508142.1:n.83+3811G=
XM_005245404.3:c.83+3811G=	XP_005245461.1:n.83+3811G=
XM_011509838.2:c.83+3811G=	XP_011508140.1:n.83+3811G=
XM_011509839.2:c.83+3811G=	XP_011508141.1:n.83+3811G=
XM_011509840.2:c.83+3811G=	XP_011508142.1:n.83+3811G=
XM_017001996.1:c.83+3811G=	XP_016857485.1:n.83+3811G=
NM_021636.3:c.57-7375G=	NP_067649.2:n.57-7375G=
NM_001017403.2:c.213-7375G= MANE Select	NP_001017403.1:n.213-7375G=
NM_001017404.2:c.83+3811G=	NP_001017404.1:n.83+3811G=