Canonical Allele Identifier: CA1982908696

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493269G= , CM000673.2:g.74493269G=	GRCh38
NC_000011.9:g.74204314G= , CM000673.1:g.74204314G=	GRCh37
NC_000011.8:g.73881962G=	NCBI36
NG_051333.1:g.5445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.435C= MANE Select	ENSP00000309463.4:p.Val145=
ENST00000310109.4:c.435C=	ENSP00000309463.4:p.Val145=
ENST00000527115.1:c.47C=
ENST00000528085.1:c.181+198C=
NM_001144869.1:c.435C=	NP_001138341.1:p.Val145=
XM_011545021.1:c.435C=	XP_011543323.1:p.Val145=
NM_001144869.2:c.435C=	NP_001138341.1:p.Val145=
NM_001329941.1:c.435C=	NP_001316870.1:p.Val145=
NM_001329942.1:c.237+198C=	NP_001316871.1:n.237+198C=
NM_001144869.3:c.435C= MANE Select	NP_001138341.1:p.Val145=
NM_001329941.2:c.435C=	NP_001316870.1:p.Val145=
NM_001329942.2:c.237+198C=	NP_001316871.1:n.237+198C=