Canonical Allele Identifier: CA424859045

Gene: LPIN1

Linked Data

• MyVariant Identifiers: chr2:g.11923968A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11783842A>C , CM000664.2:g.11783842A>C	GRCh38
NC_000002.11:g.11923968A>C , CM000664.1:g.11923968A>C	GRCh37
NC_000002.10:g.11841419A>C	NCBI36
NG_012843.2:g.111264A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674199.1:c.1278A>C MANE Select	ENSP00000501331.1:p.Arg426=
ENST00000256720.6:c.1170A>C	ENSP00000256720.2:p.Arg390=
ENST00000396097.5:c.1296A>C	ENSP00000379404.2:p.Arg432=
ENST00000396098.5:c.1296A>C	ENSP00000379405.1:p.Arg432=
ENST00000396099.5:c.1296A>C	ENSP00000379406.2:p.Arg432=
ENST00000404113.6:n.763A>C
ENST00000425416.6:c.1188A>C	ENSP00000401522.2:p.Arg396=
ENST00000449576.6:c.1425A>C	ENSP00000397908.2:p.Arg475=
ENST00000460096.1:n.158A>C
NM_001261427.1:c.1188A>C	NP_001248356.1:p.Arg396=
NM_001261428.1:c.1425A>C	NP_001248357.1:p.Arg475=
NM_001261429.1:c.1296A>C	NP_001248358.1:p.Arg432=
NM_145693.2:c.1170A>C	NP_663731.1:p.Arg390=
XM_006711869.1:c.1317A>C	XP_006711932.1:p.Arg439=
XM_006711870.2:c.1296A>C	XP_006711933.1:p.Arg432=
XM_006711871.1:c.1278A>C	XP_006711934.1:p.Arg426=
XM_006711872.1:c.1278A>C	XP_006711935.1:p.Arg426=
XM_006711874.1:c.1278A>C	XP_006711937.1:p.Arg426=
XM_011510333.1:c.1422A>C	XP_011508635.1:p.Arg474=
XM_011510334.1:c.1296A>C	XP_011508636.1:p.Arg432=
XM_011510335.1:c.1278A>C	XP_011508637.1:p.Arg426=
XM_011510336.1:c.1278A>C	XP_011508638.1:p.Arg426=
XM_011510337.1:c.1425A>C	XP_011508639.1:p.Arg475=
XM_011510338.1:c.1425A>C	XP_011508640.1:p.Arg475=
NM_001261427.2:c.1188A>C	NP_001248356.1:p.Arg396=
NM_001261428.2:c.1425A>C	NP_001248357.1:p.Arg475=
NM_001349199.1:c.1170A>C	NP_001336128.1:p.Arg390=
NM_001349200.1:c.1170A>C	NP_001336129.1:p.Arg390=
NM_001349201.1:c.1170A>C	NP_001336130.1:p.Arg390=
NM_001349202.1:c.1275A>C	NP_001336131.1:p.Arg425=
NM_001349203.1:c.1275A>C	NP_001336132.1:p.Arg425=
NM_001349204.1:c.1278A>C	NP_001336133.1:p.Arg426=
NM_001349205.1:c.1278A>C	NP_001336134.1:p.Arg426=
NM_001349206.1:c.1278A>C	NP_001336135.1:p.Arg426=
NM_001349207.1:c.1368A>C	NP_001336136.1:p.Arg456=
NM_001349208.1:c.1317A>C	NP_001336137.1:p.Arg439=
NM_145693.3:c.1170A>C	NP_663731.1:p.Arg390=
NR_146080.1:n.1266A>C
XM_006711870.4:c.1296A>C	XP_006711933.1:p.Arg432=
XM_006711872.3:c.1278A>C	XP_006711935.1:p.Arg426=
XM_011510333.2:c.1422A>C	XP_011508635.1:p.Arg474=
XM_011510334.3:c.1296A>C	XP_011508636.1:p.Arg432=
XM_011510335.3:c.1278A>C	XP_011508637.1:p.Arg426=
XM_011510336.3:c.1278A>C	XP_011508638.1:p.Arg426=
XM_017003623.2:c.1347A>C	XP_016859112.1:p.Arg449=
XM_017003624.2:c.1278A>C	XP_016859113.1:p.Arg426=
XM_017003625.2:c.1278A>C	XP_016859114.1:p.Arg426=
XM_017003627.2:c.1275A>C	XP_016859116.1:p.Arg425=
XM_017003628.2:c.1170A>C	XP_016859117.1:p.Arg390=
XM_017003629.1:c.1170A>C	XP_016859118.1:p.Arg390=
XM_017003630.2:c.1170A>C	XP_016859119.1:p.Arg390=
XM_017003631.1:c.1278A>C	XP_016859120.1:p.Arg426=
XM_024452762.1:c.1278A>C	XP_024308530.1:p.Arg426=
XM_024452763.1:c.1188A>C	XP_024308531.1:p.Arg396=
NM_001261428.3:c.1425A>C	NP_001248357.1:p.Arg475=
NM_001349199.2:c.1170A>C	NP_001336128.1:p.Arg390=
NM_001349200.2:c.1170A>C	NP_001336129.1:p.Arg390=
NM_001349201.2:c.1170A>C	NP_001336130.1:p.Arg390=
NM_001349202.2:c.1275A>C	NP_001336131.1:p.Arg425=
NM_001349203.2:c.1275A>C	NP_001336132.1:p.Arg425=
NM_001349204.2:c.1278A>C	NP_001336133.1:p.Arg426=
NM_001349206.2:c.1278A>C MANE Select	NP_001336135.1:p.Arg426=
NM_001349207.2:c.1368A>C	NP_001336136.1:p.Arg456=
NM_001349208.2:c.1317A>C	NP_001336137.1:p.Arg439=
NM_145693.4:c.1170A>C	NP_663731.1:p.Arg390=
NR_146080.2:n.1219A>C
NM_001261427.3:c.1188A>C	NP_001248356.1:p.Arg396=
NM_001349205.2:c.1278A>C	NP_001336134.1:p.Arg426=