Canonical Allele Identifier: CA381976438

Gene: LIPT2

Linked Data

• gnomAD v4: 11-74493285-G-A
• MyVariant Identifiers: chr11:g.74204330G>A (hg19) ; chr11:g.74493285G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493285G>A , CM000673.2:g.74493285G>A	GRCh38
NC_000011.9:g.74204330G>A , CM000673.1:g.74204330G>A	GRCh37
NC_000011.8:g.73881978G>A	NCBI36
NG_051333.1:g.5429C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.419C>T MANE Select	ENSP00000309463.4:p.Pro140Leu
ENST00000310109.4:c.419C>T	ENSP00000309463.4:p.Pro140Leu
ENST00000527115.1:c.31C>T
ENST00000528085.1:c.181+182C>T
NM_001144869.1:c.419C>T	NP_001138341.1:p.Pro140Leu
XM_011545021.1:c.419C>T	XP_011543323.1:p.Pro140Leu
NM_001144869.2:c.419C>T	NP_001138341.1:p.Pro140Leu
NM_001329941.1:c.419C>T	NP_001316870.1:p.Pro140Leu
NM_001329942.1:c.237+182C>T	NP_001316871.1:n.237+182C>T
NM_001144869.3:c.419C>T MANE Select	NP_001138341.1:p.Pro140Leu
NM_001329941.2:c.419C>T	NP_001316870.1:p.Pro140Leu
NM_001329942.2:c.237+182C>T	NP_001316871.1:n.237+182C>T