Canonical Allele Identifier: CA402418377

Gene: LIPG

Linked Data

• MyVariant Identifiers: chr18:g.47093814G>C (hg19) ; chr18:g.49567444G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49567444G>C , CM000680.2:g.49567444G>C	GRCh38
NC_000018.9:g.47093814G>C , CM000680.1:g.47093814G>C	GRCh37
NC_000018.8:g.45347812G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261292.9:c.282G>C MANE Select	ENSP00000261292.4:p.Met94Ile
ENST00000261292.8:c.282G>C	ENSP00000261292.4:p.Met94Ile
ENST00000427224.6:c.282G>C	ENSP00000387978.2:p.Met94Ile
ENST00000577628.5:c.390G>C	ENSP00000463835.1:p.Met130Ile
ENST00000579750.1:c.246G>C	ENSP00000462480.1:p.Met82Ile
ENST00000580036.5:c.282G>C	ENSP00000462420.1:p.Met94Ile
ENST00000583083.1:c.42G>C	ENSP00000463077.1:p.Met14Ile
NM_001308006.1:c.282G>C	NP_001294935.1:p.Met94Ile
NM_006033.2:c.282G>C	NP_006024.1:p.Met94Ile
NM_006033.3:c.282G>C	NP_006024.1:p.Met94Ile
XM_005258390.1:c.390G>C	XP_005258447.1:p.Met130Ile
XM_011526265.1:c.390G>C	XP_011524567.1:p.Met130Ile
XM_011526267.1:c.42G>C	XP_011524569.1:p.Met14Ile
XM_011526265.3:c.390G>C	XP_011524567.1:p.Met130Ile
XM_017026095.1:c.-422G>C	XP_016881584.1:n.-422G>C
NM_006033.4:c.282G>C MANE Select	NP_006024.1:p.Met94Ile
NM_001308006.2:c.282G>C	NP_001294935.1:p.Met94Ile