Canonical Allele Identifier: CA1982908706

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493284_74493285delinsCG , CM000673.2:g.74493284_74493285delinsCG	GRCh38
NC_000011.9:g.74204329_74204330delinsCG , CM000673.1:g.74204329_74204330delinsCG	GRCh37
NC_000011.8:g.73881977_73881978delinsCG	NCBI36
NG_051333.1:g.5429_5430delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.419_420delinsCG MANE Select	ENSP00000309463.4:p.Pro140=
ENST00000310109.4:c.419_420delinsCG	ENSP00000309463.4:p.Pro140=
ENST00000527115.1:c.31_32delinsCG
ENST00000528085.1:c.181+182_181+183delinsCG
NM_001144869.1:c.419_420delinsCG	NP_001138341.1:p.Pro140=
XM_011545021.1:c.419_420delinsCG	XP_011543323.1:p.Pro140=
NM_001144869.2:c.419_420delinsCG	NP_001138341.1:p.Pro140=
NM_001329941.1:c.419_420delinsCG	NP_001316870.1:p.Pro140=
NM_001329942.1:c.237+182_237+183delinsCG	NP_001316871.1:n.237+182_237+183delinsCG
NM_001144869.3:c.419_420delinsCG MANE Select	NP_001138341.1:p.Pro140=
NM_001329941.2:c.419_420delinsCG	NP_001316870.1:p.Pro140=
NM_001329942.2:c.237+182_237+183delinsCG	NP_001316871.1:n.237+182_237+183delinsCG