Canonical Allele Identifier: CA1361847134

Gene: LZTFL1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.45835591G= , CM000665.2:g.45835591G=	GRCh38
NC_000003.11:g.45877083G= , CM000665.1:g.45877083G=	GRCh37
NC_000003.10:g.45852087G=	NCBI36
NG_033917.1:g.85134C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020347.4:c.322C= MANE Select	NP_065080.1:p.Arg108=
ENST00000296135.11:c.322C= MANE Select	ENSP00000296135.6:p.Arg108=
NM_001276378.1:c.271C=	NP_001263307.1:p.Arg91=
NM_001276378.2:c.271C=	NP_001263307.1:p.Arg91=
NM_001276379.1:c.310C=	NP_001263308.1:p.Arg104=
NM_001276379.2:c.310C=	NP_001263308.1:p.Arg104=
NM_001386451.1:c.271C=	NP_001373380.1:p.Arg91=
NM_001386452.1:c.322C=	NP_001373381.1:p.Arg108=
NM_020347.3:c.322C=	NP_065080.1:p.Arg108=
NR_075080.1:n.364C=
NR_075080.2:n.325C=
ENST00000296135.10:c.322C=	ENSP00000296135.6:p.Arg108=
ENST00000411866.5:c.168C=	ENSP00000397589.1:p.Thr56=
ENST00000418700.5:c.*337C=	ENSP00000416427.1:n.*337C=
ENST00000418700.6:c.*303C=	ENSP00000416427.2:n.*303C=
ENST00000440576.2:c.194C=
ENST00000445698.1:c.271C=
ENST00000448111.5:c.*212C=	ENSP00000400177.1:n.*212C=
ENST00000469874.5:n.207C=
ENST00000480156.5:n.467C=
ENST00000490463.5:n.485C=
ENST00000490463.6:c.271C=	ENSP00000506299.2:p.Arg91=
ENST00000495864.5:n.476C=
ENST00000536047.5:c.271C=	ENSP00000439522.1:p.Arg91=
ENST00000539217.5:c.310C=	ENSP00000441784.1:p.Arg104=
ENST00000684620.1:c.271C=	ENSP00000506925.1:p.Arg91=
ENST00000699186.1:n.255C=
ENST00000699187.1:c.322C=	ENSP00000514188.1:p.Arg108=
XM_006713207.2:c.322C=	XP_006713270.2:p.Arg108=
XM_006713207.3:c.322C=	XP_006713270.2:p.Arg108=
XM_011533838.1:c.271C=	XP_011532140.1:p.Arg91=
XM_011533838.2:c.271C=	XP_011532140.1:p.Arg91=
XM_011533839.1:c.352C=	XP_011532141.1:p.Arg118=
XM_017006645.2:c.349C=	XP_016862134.1:p.Arg117=