Canonical Allele Identifier: CA1982908631

Gene: LIPT2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493177_74493178delinsGC , CM000673.2:g.74493177_74493178delinsGC	GRCh38
NC_000011.9:g.74204222_74204223delinsGC , CM000673.1:g.74204222_74204223delinsGC	GRCh37
NC_000011.8:g.73881870_73881871delinsGC	NCBI36
NG_051333.1:g.5536_5537delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+60_466+61delinsGC MANE Select	ENSP00000309463.4:n.466+60_466+61delinsGC
ENST00000310109.4:c.466+60_466+61delinsGC	ENSP00000309463.4:n.466+60_466+61delinsGC
ENST00000527115.1:c.116+22_116+23delinsGC
ENST00000528085.1:c.181+289_181+290delinsGC
NM_001144869.1:c.466+60_466+61delinsGC	NP_001138341.1:n.466+60_466+61delinsGC
XM_011545021.1:c.504+22_504+23delinsGC	XP_011543323.1:n.504+22_504+23delinsGC
NM_001144869.2:c.466+60_466+61delinsGC	NP_001138341.1:n.466+60_466+61delinsGC
NM_001329941.1:c.504+22_504+23delinsGC	NP_001316870.1:n.504+22_504+23delinsGC
NM_001329942.1:c.237+289_237+290delinsGC	NP_001316871.1:n.237+289_237+290delinsGC
NM_001144869.3:c.466+60_466+61delinsGC MANE Select	NP_001138341.1:n.466+60_466+61delinsGC
NM_001329941.2:c.504+22_504+23delinsGC	NP_001316870.1:n.504+22_504+23delinsGC
NM_001329942.2:c.237+289_237+290delinsGC	NP_001316871.1:n.237+289_237+290delinsGC