Canonical Allele Identifier: CA2615095511

Gene: LIPT2

Linked Data

• gnomAD v4: 11-74493179-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74493179C>G , CM000673.2:g.74493179C>G	GRCh38
NC_000011.9:g.74204224C>G , CM000673.1:g.74204224C>G	GRCh37
NC_000011.8:g.73881872C>G	NCBI36
NG_051333.1:g.5535G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310109.5:c.466+59G>C MANE Select	ENSP00000309463.4:n.466+59G>C
ENST00000310109.4:c.466+59G>C	ENSP00000309463.4:n.466+59G>C
ENST00000527115.1:c.116+21G>C
ENST00000528085.1:c.181+288G>C
NM_001144869.1:c.466+59G>C	NP_001138341.1:n.466+59G>C
XM_011545021.1:c.504+21G>C	XP_011543323.1:n.504+21G>C
NM_001144869.2:c.466+59G>C	NP_001138341.1:n.466+59G>C
NM_001329941.1:c.504+21G>C	NP_001316870.1:n.504+21G>C
NM_001329942.1:c.237+288G>C	NP_001316871.1:n.237+288G>C
NM_001144869.3:c.466+59G>C MANE Select	NP_001138341.1:n.466+59G>C
NM_001329941.2:c.504+21G>C	NP_001316870.1:n.504+21G>C
NM_001329942.2:c.237+288G>C	NP_001316871.1:n.237+288G>C