Canonical Allele Identifier: CA1361847147

Gene: LZTFL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45835653A= , CM000665.2:g.45835653A=	GRCh38
NC_000003.11:g.45877145A= , CM000665.1:g.45877145A=	GRCh37
NC_000003.10:g.45852149A=	NCBI36
NG_033917.1:g.85072T=

Transcript Alleles

HGVS	Amino-acid Change
NM_020347.4:c.260T= MANE Select	NP_065080.1:p.Leu87=
ENST00000296135.11:c.260T= MANE Select	ENSP00000296135.6:p.Leu87=
NM_001276378.1:c.209T=	NP_001263307.1:p.Leu70=
NM_001276378.2:c.209T=	NP_001263307.1:p.Leu70=
NM_001276379.1:c.248T=	NP_001263308.1:p.Leu83=
NM_001276379.2:c.248T=	NP_001263308.1:p.Leu83=
NM_001386451.1:c.209T=	NP_001373380.1:p.Leu70=
NM_001386452.1:c.260T=	NP_001373381.1:p.Leu87=
NM_020347.3:c.260T=	NP_065080.1:p.Leu87=
NR_075080.1:n.302T=
NR_075080.2:n.263T=
ENST00000296135.10:c.260T=	ENSP00000296135.6:p.Leu87=
ENST00000411866.5:c.106T=	ENSP00000397589.1:p.Cys36=
ENST00000418700.5:c.*275T=	ENSP00000416427.1:n.*275T=
ENST00000418700.6:c.*241T=	ENSP00000416427.2:n.*241T=
ENST00000440576.2:c.132T=
ENST00000445698.1:c.209T=	ENSP00000412240.1:p.Leu70=
ENST00000448111.5:c.*150T=	ENSP00000400177.1:n.*150T=
ENST00000469874.5:n.145T=
ENST00000480156.5:n.405T=
ENST00000490463.5:n.423T=
ENST00000490463.6:c.209T=	ENSP00000506299.2:p.Leu70=
ENST00000495864.5:n.414T=
ENST00000536047.5:c.209T=	ENSP00000439522.1:p.Leu70=
ENST00000539217.5:c.248T=	ENSP00000441784.1:p.Leu83=
ENST00000684620.1:c.209T=	ENSP00000506925.1:p.Leu70=
ENST00000699186.1:n.193T=
ENST00000699187.1:c.260T=	ENSP00000514188.1:p.Leu87=
XM_006713207.2:c.260T=	XP_006713270.2:p.Leu87=
XM_006713207.3:c.260T=	XP_006713270.2:p.Leu87=
XM_011533838.1:c.209T=	XP_011532140.1:p.Leu70=
XM_011533838.2:c.209T=	XP_011532140.1:p.Leu70=
XM_011533839.1:c.290T=	XP_011532141.1:p.Leu97=
XM_017006645.2:c.287T=	XP_016862134.1:p.Leu96=