Canonical Allele Identifier: CA1982908689

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493257A= , CM000673.2:g.74493257A=	GRCh38
NC_000011.9:g.74204302A= , CM000673.1:g.74204302A=	GRCh37
NC_000011.8:g.73881950A=	NCBI36
NG_051333.1:g.5457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.447T= MANE Select	ENSP00000309463.4:p.Asp149=
ENST00000310109.4:c.447T=	ENSP00000309463.4:p.Asp149=
ENST00000527115.1:c.59T=
ENST00000528085.1:c.181+210T=
NM_001144869.1:c.447T=	NP_001138341.1:p.Asp149=
XM_011545021.1:c.447T=	XP_011543323.1:p.Asp149=
NM_001144869.2:c.447T=	NP_001138341.1:p.Asp149=
NM_001329941.1:c.447T=	NP_001316870.1:p.Asp149=
NM_001329942.1:c.237+210T=	NP_001316871.1:n.237+210T=
NM_001144869.3:c.447T= MANE Select	NP_001138341.1:p.Asp149=
NM_001329941.2:c.447T=	NP_001316870.1:p.Asp149=
NM_001329942.2:c.237+210T=	NP_001316871.1:n.237+210T=