Canonical Allele Identifier: CA10641288

Gene: LPIN2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3011774G>A , CM000680.2:g.3011774G>A	GRCh38
NC_000018.9:g.3011772G>A , CM000680.1:g.3011772G>A	GRCh37
NC_000018.8:g.3001772G>A	NCBI36
NG_007507.1:g.5174C>T , LRG_174:g.5174C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261596.9:c.-66C>T	ENSP00000261596.4:n.-66C>T
ENST00000697039.1:c.-10+1313C>T	ENSP00000513061.1:n.-10+1313C>T
ENST00000697040.1:c.-10+1263C>T	ENSP00000513062.1:n.-10+1263C>T
ENST00000677752.1:c.-10+1313C>T MANE Select	ENSP00000504857.1:n.-10+1313C>T
ENST00000261596.8:c.-66C>T	ENSP00000261596.4:n.-66C>T
ENST00000584294.1:c.-10+1313C>T	ENSP00000463026.1:n.-10+1313C>T
NM_014646.2:c.-66C>T , LRG_174t1:c.-66C>T	NP_055461.1:n.-66C>T
XM_005258178.2:c.-10+1313C>T	XP_005258235.1:n.-10+1313C>T
XM_005258179.3:c.-10+1263C>T	XP_005258236.1:n.-10+1263C>T
XR_935074.1:n.120+1263C>T
XM_005258178.3:c.-10+1313C>T	XP_005258235.1:n.-10+1313C>T
XM_005258179.5:c.-10+1263C>T	XP_005258236.1:n.-10+1263C>T
XM_017026098.1:c.-66C>T	XP_016881587.1:n.-66C>T
XR_935074.2:n.165+1263C>T
NM_001375808.1:c.-10+1313C>T	NP_001362737.1:n.-10+1313C>T
NM_001375809.1:c.-10+1263C>T	NP_001362738.1:n.-10+1263C>T
NM_001375808.2:c.-10+1313C>T MANE Select	NP_001362737.1:n.-10+1313C>T