Canonical Allele Identifier: CA42596938

Gene: LPIN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.11713457G>T , CM000664.2:g.11713457G>T	GRCh38
NC_000002.11:g.11853583G>T , CM000664.1:g.11853583G>T	GRCh37
NC_000002.10:g.11771034G>T	NCBI36
NG_012843.2:g.40879G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001261428.1:c.82-299G>T	NP_001248357.1:n.82-299G>T
NM_001261428.2:c.82-299G>T	NP_001248357.1:n.82-299G>T
NM_001261428.3:c.82-299G>T	NP_001248357.1:n.82-299G>T
NM_001349207.1:c.81+35729G>T	NP_001336136.1:n.81+35729G>T
NM_001349207.2:c.81+35729G>T	NP_001336136.1:n.81+35729G>T
NM_001349208.1:c.82-299G>T	NP_001336137.1:n.82-299G>T
NM_001349208.2:c.82-299G>T	NP_001336137.1:n.82-299G>T
ENST00000449576.6:c.82-299G>T	ENSP00000397908.2:n.82-299G>T
XM_006711869.1:c.82-299G>T	XP_006711932.1:n.82-299G>T
XM_011510333.1:c.82-299G>T	XP_011508635.1:n.82-299G>T
XM_011510333.2:c.82-299G>T	XP_011508635.1:n.82-299G>T
XM_011510337.1:c.82-299G>T	XP_011508639.1:n.82-299G>T
XM_011510338.1:c.82-299G>T	XP_011508640.1:n.82-299G>T
XM_017003623.2:c.4-299G>T	XP_016859112.1:n.4-299G>T