Canonical Allele Identifier: CA2765048234

Gene: LPCAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1518304C>G , CM000667.2:g.1518304C>G	GRCh38
NC_000005.9:g.1518419C>G , CM000667.1:g.1518419C>G	GRCh37
NC_000005.8:g.1571419C>G	NCBI36
NG_051622.1:g.10674G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283415.4:c.135+5406G>C MANE Select	ENSP00000283415.3:n.135+5406G>C
ENST00000283415.3:c.135+5406G>C	ENSP00000283415.3:n.135+5406G>C
ENST00000475622.5:c.135+5406G>C	ENSP00000423472.1:n.135+5406G>C
ENST00000514484.6:n.165+3043G>C
NM_024830.3:c.135+5406G>C	NP_079106.3:n.135+5406G>C
XM_005248373.2:c.-10+3043G>C	XP_005248430.1:n.-10+3043G>C
XM_011514133.1:c.201+7211G>C	XP_011512435.1:n.201+7211G>C
NM_024830.4:c.135+5406G>C	NP_079106.3:n.135+5406G>C
XM_005248373.3:c.-10+3043G>C	XP_005248430.1:n.-10+3043G>C
NM_024830.5:c.135+5406G>C MANE Select	NP_079106.3:n.135+5406G>C