Canonical Allele Identifier: CA10647387

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2918551T>C , CM000680.2:g.2918551T>C	GRCh38
NC_000018.9:g.2918549T>C , CM000680.1:g.2918549T>C	GRCh37
NC_000018.8:g.2908549T>C	NCBI36
NG_007507.1:g.98397A>G , LRG_174:g.98397A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.*1742A>G	ENSP00000261596.4:n.*1742A>G
ENST00000697039.1:c.2546+2227A>G	ENSP00000513061.1:n.2546+2227A>G
ENST00000697040.1:c.*1742A>G	ENSP00000513062.1:n.*1742A>G
ENST00000697041.1:c.3468A>G	ENSP00000513063.1:n.3468A>G
ENST00000677752.1:c.*1742A>G MANE Select	ENSP00000504857.1:n.*1742A>G
ENST00000261596.8:c.*1742A>G	ENSP00000261596.4:n.*1742A>G
NM_014646.2:c.*1742A>G , LRG_174t1:c.*1742A>G	NP_055461.1:n.*1742A>G
XM_005258177.3:c.*1742A>G	XP_005258234.1:n.*1742A>G
XM_005258178.2:c.*1742A>G	XP_005258235.1:n.*1742A>G
XM_005258179.3:c.*1742A>G	XP_005258236.1:n.*1742A>G
XM_005258177.4:c.*1742A>G	XP_005258234.1:n.*1742A>G
XM_005258178.3:c.*1742A>G	XP_005258235.1:n.*1742A>G
XM_005258179.5:c.*1742A>G	XP_005258236.1:n.*1742A>G
XM_017026098.1:c.*1742A>G	XP_016881587.1:n.*1742A>G
XM_017026099.1:c.*1742A>G	XP_016881588.1:n.*1742A>G
NM_001375808.1:c.*1742A>G	NP_001362737.1:n.*1742A>G
NM_001375809.1:c.*1742A>G	NP_001362738.1:n.*1742A>G
NM_001375808.2:c.*1742A>G MANE Select	NP_001362737.1:n.*1742A>G