Canonical Allele Identifier: CA1413543477

Gene: LEKR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.156838195T= , CM000665.2:g.156838195T=	GRCh38
NC_000003.11:g.156555984T= , CM000665.1:g.156555984T=	GRCh37
NC_000003.10:g.158038678T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356539.9:c.48+8818T= MANE Select	ENSP00000348936.4:n.48+8818T=
ENST00000470811.6:c.48+8818T=	ENSP00000418214.2:n.48+8818T=
ENST00000356539.8:c.48+8818T=	ENSP00000348936.4:n.48+8818T=
ENST00000465728.5:n.273+8818T=
ENST00000467376.5:n.135+8818T=
ENST00000470811.5:c.-1174+8818T=	ENSP00000418214.1:n.-1174+8818T=
ENST00000477399.5:c.48+8818T=	ENSP00000425282.1:n.48+8818T=
ENST00000483177.5:c.48+8818T=	ENSP00000421730.1:n.48+8818T=
ENST00000485017.1:n.291+8818T=
ENST00000489350.5:n.140+8818T=
ENST00000491763.1:c.48+8818T=	ENSP00000474182.1:n.48+8818T=
ENST00000498839.5:c.48+8818T=	ENSP00000425746.1:n.48+8818T=
NM_001004316.2:c.48+8818T=	NP_001004316.2:n.48+8818T=
NM_001193283.1:c.48+8818T=	NP_001180212.1:n.48+8818T=
XM_005247441.2:c.48+8818T=	XP_005247498.1:n.48+8818T=
XM_005247442.2:c.48+8818T=	XP_005247499.1:n.48+8818T=
XM_006713631.2:c.549+8818T=	XP_006713694.1:n.549+8818T=
XM_006713632.2:c.549+8818T=	XP_006713695.1:n.549+8818T=
XM_011512803.1:c.549+8818T=	XP_011511105.1:n.549+8818T=
XM_011512804.1:c.48+8818T=	XP_011511106.1:n.48+8818T=
XM_011512806.1:c.549+8818T=	XP_011511108.1:n.549+8818T=
XM_011512807.1:c.549+8818T=	XP_011511109.1:n.549+8818T=
XM_011512808.1:c.549+8818T=	XP_011511110.1:n.549+8818T=
XM_011512811.1:c.549+8818T=	XP_011511113.1:n.549+8818T=
XM_011512812.1:c.549+8818T=	XP_011511114.1:n.549+8818T=
XM_011512814.1:c.-57+8818T=	XP_011511116.1:n.-57+8818T=
XM_011512815.1:c.549+8818T=	XP_011511117.1:n.549+8818T=
XM_011512816.1:c.549+8818T=	XP_011511118.1:n.549+8818T=
XR_924134.1:n.590+8818T=
XR_924135.1:n.590+8818T=
XM_005247441.4:c.48+8818T=	XP_005247498.1:n.48+8818T=
XM_005247442.4:c.48+8818T=	XP_005247499.1:n.48+8818T=
XM_006713631.3:c.549+8818T=	XP_006713694.1:n.549+8818T=
XM_011512803.2:c.549+8818T=	XP_011511105.1:n.549+8818T=
XM_011512804.3:c.48+8818T=	XP_011511106.1:n.48+8818T=
XM_011512806.2:c.549+8818T=	XP_011511108.1:n.549+8818T=
XM_011512807.2:c.549+8818T=	XP_011511109.1:n.549+8818T=
XM_011512808.2:c.549+8818T=	XP_011511110.1:n.549+8818T=
XM_011512811.2:c.549+8818T=	XP_011511113.1:n.549+8818T=
XM_011512814.2:c.-57+8818T=	XP_011511116.1:n.-57+8818T=
XM_011512815.2:c.549+8818T=	XP_011511117.1:n.549+8818T=
XM_011512816.2:c.549+8818T=	XP_011511118.1:n.549+8818T=
XM_017006375.1:c.-66+8818T=	XP_016861864.1:n.-66+8818T=
XR_924134.2:n.686+8818T=
XR_924135.3:n.686+8818T=
NM_001193283.2:c.48+8818T=	NP_001180212.1:n.48+8818T=
NM_001004316.3:c.48+8818T= MANE Select	NP_001004316.2:n.48+8818T=