Canonical Allele Identifier: CA355688113

Gene: LIPH

Linked Data

• MyVariant Identifiers: chr3:g.185236984T>C (hg19) ; chr3:g.185519196T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.185519196T>C , CM000665.2:g.185519196T>C	GRCh38
NC_000003.11:g.185236984T>C , CM000665.1:g.185236984T>C	GRCh37
NC_000003.10:g.186719678T>C	NCBI36
NG_012183.1:g.38386A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296252.9:c.832A>G MANE Select	ENSP00000296252.4:p.Asn278Asp
ENST00000296252.8:c.832A>G	ENSP00000296252.4:p.Asn278Asp
ENST00000424591.6:c.730A>G	ENSP00000396384.2:p.Asn244Asp
ENST00000452897.1:c.204A>G
NM_139248.2:c.832A>G	NP_640341.1:p.Asn278Asp
XM_006713529.2:c.742A>G	XP_006713592.1:p.Asn248Asp
XM_011512530.1:c.703A>G	XP_011510832.1:p.Asn235Asp
XM_011512531.1:c.703A>G	XP_011510833.1:p.Asn235Asp
XM_006713529.4:c.742A>G	XP_006713592.1:p.Asn248Asp
XM_011512530.3:c.703A>G	XP_011510832.1:p.Asn235Asp
XM_011512531.3:c.703A>G	XP_011510833.1:p.Asn235Asp
XM_017005852.2:c.730A>G	XP_016861341.1:p.Asn244Asp
NM_139248.3:c.832A>G MANE Select	NP_640341.1:p.Asn278Asp