Canonical Allele Identifier: CA381976745

Gene: LIPT2 LIPT2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493441A>C , CM000673.2:g.74493441A>C	GRCh38
NC_000011.9:g.74204486A>C , CM000673.1:g.74204486A>C	GRCh37
NC_000011.8:g.73882134A>C	NCBI36
NG_051333.1:g.5273T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001144869.3:c.263T>G (LIPT2) MANE Select	NP_001138341.1:p.Leu88Arg
ENST00000310109.5:c.263T>G (LIPT2) MANE Select	ENSP00000309463.4:p.Leu88Arg
NM_001144869.1:c.263T>G (LIPT2)	NP_001138341.1:p.Leu88Arg
NM_001144869.2:c.263T>G (LIPT2)	NP_001138341.1:p.Leu88Arg
NM_001319240.1:c.-790A>C (LIPT2-AS1)	NP_001306169.1:n.-790A>C
NM_001329941.1:c.263T>G (LIPT2)	NP_001316870.1:p.Leu88Arg
NM_001329941.2:c.263T>G (LIPT2)	NP_001316870.1:p.Leu88Arg
NM_001329942.1:c.237+26T>G (LIPT2)	NP_001316871.1:n.237+26T>G
NM_001329942.2:c.237+26T>G (LIPT2)	NP_001316871.1:n.237+26T>G
NR_171028.1:n.62A>C (LIPT2-AS1)
ENST00000310109.4:c.263T>G (LIPT2)	ENSP00000309463.4:p.Leu88Arg
ENST00000528085.1:c.181+26T>G (LIPT2)
XM_011545021.1:c.263T>G (LIPT2)	XP_011543323.1:p.Leu88Arg
XR_132892.1:n.2A>C (LIPT2-AS1)