Canonical Allele Identifier: CA2615095493

Gene: LIPT2

Linked Data

• gnomAD v4: 11-74493171-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493171G>T , CM000673.2:g.74493171G>T	GRCh38
NC_000011.9:g.74204216G>T , CM000673.1:g.74204216G>T	GRCh37
NC_000011.8:g.73881864G>T	NCBI36
NG_051333.1:g.5543C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+67C>A MANE Select	ENSP00000309463.4:n.466+67C>A
ENST00000310109.4:c.466+67C>A	ENSP00000309463.4:n.466+67C>A
ENST00000527115.1:c.116+29C>A
ENST00000528085.1:c.181+296C>A
NM_001144869.1:c.466+67C>A	NP_001138341.1:n.466+67C>A
XM_011545021.1:c.504+29C>A	XP_011543323.1:n.504+29C>A
NM_001144869.2:c.466+67C>A	NP_001138341.1:n.466+67C>A
NM_001329941.1:c.504+29C>A	NP_001316870.1:n.504+29C>A
NM_001329942.1:c.237+296C>A	NP_001316871.1:n.237+296C>A
NM_001144869.3:c.466+67C>A MANE Select	NP_001138341.1:n.466+67C>A
NM_001329941.2:c.504+29C>A	NP_001316870.1:n.504+29C>A
NM_001329942.2:c.237+296C>A	NP_001316871.1:n.237+296C>A