Canonical Allele Identifier: CA1982908629

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493172A= , CM000673.2:g.74493172A=	GRCh38
NC_000011.9:g.74204217A= , CM000673.1:g.74204217A=	GRCh37
NC_000011.8:g.73881865A=	NCBI36
NG_051333.1:g.5542T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+66T= MANE Select	ENSP00000309463.4:n.466+66T=
ENST00000310109.4:c.466+66T=	ENSP00000309463.4:n.466+66T=
ENST00000527115.1:c.116+28T=
ENST00000528085.1:c.181+295T=
NM_001144869.1:c.466+66T=	NP_001138341.1:n.466+66T=
XM_011545021.1:c.504+28T=	XP_011543323.1:n.504+28T=
NM_001144869.2:c.466+66T=	NP_001138341.1:n.466+66T=
NM_001329941.1:c.504+28T=	NP_001316870.1:n.504+28T=
NM_001329942.1:c.237+295T=	NP_001316871.1:n.237+295T=
NM_001144869.3:c.466+66T= MANE Select	NP_001138341.1:n.466+66T=
NM_001329941.2:c.504+28T=	NP_001316870.1:n.504+28T=
NM_001329942.2:c.237+295T=	NP_001316871.1:n.237+295T=