Canonical Allele Identifier: CA1982908669

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493229G= , CM000673.2:g.74493229G=	GRCh38
NC_000011.9:g.74204274G= , CM000673.1:g.74204274G=	GRCh37
NC_000011.8:g.73881922G=	NCBI36
NG_051333.1:g.5485C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+9C= MANE Select	ENSP00000309463.4:n.466+9C=
ENST00000310109.4:c.466+9C=	ENSP00000309463.4:n.466+9C=
ENST00000527115.1:c.87C=
ENST00000528085.1:c.181+238C=
NM_001144869.1:c.466+9C=	NP_001138341.1:n.466+9C=
XM_011545021.1:c.475C=	XP_011543323.1:p.Arg159=
NM_001144869.2:c.466+9C=	NP_001138341.1:n.466+9C=
NM_001329941.1:c.475C=	NP_001316870.1:p.Arg159=
NM_001329942.1:c.237+238C=	NP_001316871.1:n.237+238C=
NM_001144869.3:c.466+9C= MANE Select	NP_001138341.1:n.466+9C=
NM_001329941.2:c.475C=	NP_001316870.1:p.Arg159=
NM_001329942.2:c.237+238C=	NP_001316871.1:n.237+238C=