Canonical Allele Identifier: CA10611937
Gene: LPIN1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 330940
ClinVar RCV Id: RCV000363530
dbSNP Id: rs11524

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.11826191T>C , CM000664.2:g.11826191T>C GRCh38
NC_000002.11:g.11966317T>C , CM000664.1:g.11966317T>C GRCh37
NC_000002.10:g.11883768T>C NCBI36
NG_012843.2:g.153613T>C

Transcript Alleles

HGVS Amino-acid change
NM_001261427.1:c.*1400T>C VV NP_001248356.1:p.=
NM_001261428.1:c.*1400T>C VV NP_001248357.1:p.=
NM_145693.2:c.*1400T>C VV NP_663731.1:p.=
XM_006711869.1:c.*1400T>C XP_006711932.1:p.=
XM_006711870.2:c.*1400T>C XP_006711933.1:p.=
XM_006711871.1:c.*1400T>C XP_006711934.1:p.=
XM_006711872.1:c.*1400T>C XP_006711935.1:p.=
XM_006711874.1:c.*1400T>C XP_006711937.1:p.=
XM_011510333.1:c.*1400T>C XP_011508635.1:p.=
XM_011510334.1:c.*1400T>C XP_011508636.1:p.=
XM_011510335.1:c.*1400T>C XP_011508637.1:p.=
XM_011510336.1:c.*1400T>C XP_011508638.1:p.=
NM_001261427.2:c.*1400T>C VV
NM_001261428.2:c.*1400T>C VV
NM_001349199.1:c.*1400T>C VV NP_001336128.1:p.=
NM_001349200.1:c.*1400T>C VV NP_001336129.1:p.=
NM_001349201.1:c.*1400T>C VV NP_001336130.1:p.=
NM_001349202.1:c.*1400T>C VV NP_001336131.1:p.=
NM_001349203.1:c.*1400T>C VV NP_001336132.1:p.=
NM_001349204.1:c.*1400T>C VV NP_001336133.1:p.=
NM_001349205.1:c.*1400T>C VV NP_001336134.1:p.=
NM_001349206.1:c.*1400T>C VV NP_001336135.1:p.=
NM_001349207.1:c.*1400T>C VV NP_001336136.1:p.=
NM_001349208.1:c.*1400T>C VV NP_001336137.1:p.=
NM_145693.3:c.*1400T>C VV
NR_146080.1:n.4321T>C
XM_006711870.4:c.*1400T>C
XM_006711872.3:c.*1400T>C
XM_011510334.3:c.*1400T>C
XM_011510335.3:c.*1400T>C
XM_011510336.3:c.*1400T>C
XM_017003623.2:c.*1400T>C XP_016859112.1:p.=
XM_017003624.2:c.*1400T>C XP_016859113.1:p.=
XM_017003625.2:c.*1400T>C XP_016859114.1:p.=
XM_017003627.2:c.*1400T>C XP_016859116.1:p.=
XM_017003628.2:c.*1400T>C XP_016859117.1:p.=
XM_024452762.1:c.*1400T>C XP_024308530.1:p.=
ENST00000256720.6:c.*1400T>C ENSP00000256720.2:p.=
ENST00000396097.5:c.*1400T>C ENSP00000379404.2:p.=
ENST00000404113.6:n.3666T>C
ENST00000425416.6:c.*1400T>C ENSP00000401522.2:p.=
ENST00000475922.1:n.5110T>C