Canonical Allele Identifier: CA10647393

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2919488G>C , CM000680.2:g.2919488G>C	GRCh38
NC_000018.9:g.2919486G>C , CM000680.1:g.2919486G>C	GRCh37
NC_000018.8:g.2909486G>C	NCBI36
NG_007507.1:g.97460C>G , LRG_174:g.97460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.*805C>G	ENSP00000261596.4:n.*805C>G
ENST00000697039.1:c.2546+1290C>G	ENSP00000513061.1:n.2546+1290C>G
ENST00000697040.1:c.*805C>G	ENSP00000513062.1:n.*805C>G
ENST00000697041.1:c.2531C>G	ENSP00000513063.1:n.2531C>G
ENST00000677752.1:c.*805C>G MANE Select	ENSP00000504857.1:n.*805C>G
ENST00000261596.8:c.*805C>G	ENSP00000261596.4:n.*805C>G
NM_014646.2:c.*805C>G , LRG_174t1:c.*805C>G	NP_055461.1:n.*805C>G
XM_005258177.3:c.*805C>G	XP_005258234.1:n.*805C>G
XM_005258178.2:c.*805C>G	XP_005258235.1:n.*805C>G
XM_005258179.3:c.*805C>G	XP_005258236.1:n.*805C>G
XM_005258177.4:c.*805C>G	XP_005258234.1:n.*805C>G
XM_005258178.3:c.*805C>G	XP_005258235.1:n.*805C>G
XM_005258179.5:c.*805C>G	XP_005258236.1:n.*805C>G
XM_017026098.1:c.*805C>G	XP_016881587.1:n.*805C>G
XM_017026099.1:c.*805C>G	XP_016881588.1:n.*805C>G
NM_001375808.1:c.*805C>G	NP_001362737.1:n.*805C>G
NM_001375809.1:c.*805C>G	NP_001362738.1:n.*805C>G
NM_001375808.2:c.*805C>G MANE Select	NP_001362737.1:n.*805C>G