Canonical Allele Identifier: CA987245641
Gene: LPIN2 HGNC NCBI

Linked Data

dbSNP Id: rs2077063827

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.2922108_2922109del , CM000680.2:g.2922108_2922109del GRCh38
NC_000018.9:g.2922106_2922107del , CM000680.1:g.2922106_2922107del GRCh37
NC_000018.8:g.2912106_2912107del NCBI36
NG_007507.1:g.94841_94842del , LRG_174:g.94841_94842del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261596.9:c.2267_2268del ENSP00000261596.4:p.Thr756AsnfsTer?
ENST00000697039.1:c.2267_2268del ENSP00000513061.1:p.Thr756AsnfsTer?
ENST00000697040.1:c.2267_2268del ENSP00000513062.1:p.Thr756AsnfsTer?
ENST00000697041.1:c.962_963del ENSP00000513063.1:p.Thr321AsnfsTer?
ENST00000677752.1:c.2267_2268del MANE Select ENSP00000504857.1:p.Thr756AsnfsTer?
ENST00000261596.8:c.2267_2268del ENSP00000261596.4:p.Thr756AsnfsTer?
NM_014646.2:c.2267_2268del , LRG_174t1:c.2267_2268del NP_055461.1:p.Thr756AsnfsTer?
XM_005258177.3:c.2378_2379del XP_005258234.1:p.Thr793AsnfsTer?
XM_005258178.2:c.2267_2268del XP_005258235.1:p.Thr756AsnfsTer?
XM_005258179.3:c.2267_2268del XP_005258236.1:p.Thr756AsnfsTer?
XM_005258177.4:c.2378_2379del XP_005258234.1:p.Thr793AsnfsTer?
XM_005258178.3:c.2267_2268del XP_005258235.1:p.Thr756AsnfsTer?
XM_005258179.5:c.2267_2268del XP_005258236.1:p.Thr756AsnfsTer?
XM_017026098.1:c.2267_2268del XP_016881587.1:p.Thr756AsnfsTer?
XM_017026099.1:c.2267_2268del XP_016881588.1:p.Thr756AsnfsTer?
NM_001375808.1:c.2267_2268del NP_001362737.1:p.Thr756AsnfsTer?
NM_001375809.1:c.2267_2268del NP_001362738.1:p.Thr756AsnfsTer?
NM_001375808.2:c.2267_2268del MANE Select NP_001362737.1:p.Thr756AsnfsTer?