Canonical Allele Identifier: CA437347247

Gene: LIPH

Linked Data

• MyVariant Identifiers: chr3:g.185236979G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185519191G>A , CM000665.2:g.185519191G>A	GRCh38
NC_000003.11:g.185236979G>A , CM000665.1:g.185236979G>A	GRCh37
NC_000003.10:g.186719673G>A	NCBI36
NG_012183.1:g.38391C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296252.9:c.837C>T MANE Select	ENSP00000296252.4:p.Gly279=
ENST00000296252.8:c.837C>T	ENSP00000296252.4:p.Gly279=
ENST00000424591.6:c.735C>T	ENSP00000396384.2:p.Gly245=
ENST00000452897.1:c.209C>T
NM_139248.2:c.837C>T	NP_640341.1:p.Gly279=
XM_006713529.2:c.747C>T	XP_006713592.1:p.Gly249=
XM_011512530.1:c.708C>T	XP_011510832.1:p.Gly236=
XM_011512531.1:c.708C>T	XP_011510833.1:p.Gly236=
XM_006713529.4:c.747C>T	XP_006713592.1:p.Gly249=
XM_011512530.3:c.708C>T	XP_011510832.1:p.Gly236=
XM_011512531.3:c.708C>T	XP_011510833.1:p.Gly236=
XM_017005852.2:c.735C>T	XP_016861341.1:p.Gly245=
NM_139248.3:c.837C>T MANE Select	NP_640341.1:p.Gly279=