Canonical Allele Identifier: CA381976329

Gene: LIPT2

Linked Data

• gnomAD v4: 11-74493237-C-A
• MyVariant Identifiers: chr11:g.74204282C>A (hg19) ; chr11:g.74493237C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493237C>A , CM000673.2:g.74493237C>A	GRCh38
NC_000011.9:g.74204282C>A , CM000673.1:g.74204282C>A	GRCh37
NC_000011.8:g.73881930C>A	NCBI36
NG_051333.1:g.5477G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+1G>T MANE Select	ENSP00000309463.4:n.466+1G>T
ENST00000310109.4:c.466+1G>T	ENSP00000309463.4:n.466+1G>T
ENST00000527115.1:c.79G>T
ENST00000528085.1:c.181+230G>T
NM_001144869.1:c.466+1G>T	NP_001138341.1:n.466+1G>T
XM_011545021.1:c.467G>T	XP_011543323.1:p.Gly156Val
NM_001144869.2:c.466+1G>T	NP_001138341.1:n.466+1G>T
NM_001329941.1:c.467G>T	NP_001316870.1:p.Gly156Val
NM_001329942.1:c.237+230G>T	NP_001316871.1:n.237+230G>T
NM_001144869.3:c.466+1G>T MANE Select	NP_001138341.1:n.466+1G>T
NM_001329941.2:c.467G>T	NP_001316870.1:p.Gly156Val
NM_001329942.2:c.237+230G>T	NP_001316871.1:n.237+230G>T