Canonical Allele Identifier: CA10650639

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.2917603_2917608del , CM000680.2:g.2917603_2917608del	GRCh38
NC_000018.9:g.2917601_2917606del , CM000680.1:g.2917601_2917606del	GRCh37
NC_000018.8:g.2907601_2907606del	NCBI36
NG_007507.1:g.99346_99351del , LRG_174:g.99346_99351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.*2691_*2696del	ENSP00000261596.4:n.*2691_*2696del
ENST00000697039.1:c.2546+3176_2546+3181del	ENSP00000513061.1:n.2546+3176_2546+3181del
ENST00000697040.1:c.*2691_*2696del	ENSP00000513062.1:n.*2691_*2696del
ENST00000697041.1:c.4417_4422del	ENSP00000513063.1:n.4417_4422del
ENST00000677752.1:c.*2691_*2696del MANE Select	ENSP00000504857.1:n.*2691_*2696del
ENST00000261596.8:c.*2691_*2696del	ENSP00000261596.4:n.*2691_*2696del
NM_014646.2:c.*2691_*2696del , LRG_174t1:c.*2691_*2696del	NP_055461.1:n.*2691_*2696del
XM_005258177.3:c.*2691_*2696del	XP_005258234.1:n.*2691_*2696del
XM_005258178.2:c.*2691_*2696del	XP_005258235.1:n.*2691_*2696del
XM_005258179.3:c.*2691_*2696del	XP_005258236.1:n.*2691_*2696del
XM_005258177.4:c.*2691_*2696del	XP_005258234.1:n.*2691_*2696del
XM_005258178.3:c.*2691_*2696del	XP_005258235.1:n.*2691_*2696del
XM_005258179.5:c.*2691_*2696del	XP_005258236.1:n.*2691_*2696del
XM_017026098.1:c.*2691_*2696del	XP_016881587.1:n.*2691_*2696del
XM_017026099.1:c.*2691_*2696del	XP_016881588.1:n.*2691_*2696del
NM_001375808.1:c.*2691_*2696del	NP_001362737.1:n.*2691_*2696del
NM_001375809.1:c.*2691_*2696del	NP_001362738.1:n.*2691_*2696del
NM_001375808.2:c.*2691_*2696del MANE Select	NP_001362737.1:n.*2691_*2696del