Canonical Allele Identifier: CA1982908659

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493216C= , CM000673.2:g.74493216C=	GRCh38
NC_000011.9:g.74204261C= , CM000673.1:g.74204261C=	GRCh37
NC_000011.8:g.73881909C=	NCBI36
NG_051333.1:g.5498G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+22G= MANE Select	ENSP00000309463.4:n.466+22G=
ENST00000310109.4:c.466+22G=	ENSP00000309463.4:n.466+22G=
ENST00000527115.1:c.100G=
ENST00000528085.1:c.181+251G=
NM_001144869.1:c.466+22G=	NP_001138341.1:n.466+22G=
XM_011545021.1:c.488G=	XP_011543323.1:p.Arg163=
NM_001144869.2:c.466+22G=	NP_001138341.1:n.466+22G=
NM_001329941.1:c.488G=	NP_001316870.1:p.Arg163=
NM_001329942.1:c.237+251G=	NP_001316871.1:n.237+251G=
NM_001144869.3:c.466+22G= MANE Select	NP_001138341.1:n.466+22G=
NM_001329941.2:c.488G=	NP_001316870.1:p.Arg163=
NM_001329942.2:c.237+251G=	NP_001316871.1:n.237+251G=