Canonical Allele Identifier: CA1522689916

Gene: LPCAT1

Linked Data

• dbSNP Id: rs530812114

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1518404G>T , CM000667.2:g.1518404G>T	GRCh38
NC_000005.9:g.1518519G>T , CM000667.1:g.1518519G>T	GRCh37
NC_000005.8:g.1571519G>T	NCBI36
NG_051622.1:g.10574C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000283415.4:c.135+5306C>A MANE Select	ENSP00000283415.3:n.135+5306C>A
ENST00000283415.3:c.135+5306C>A	ENSP00000283415.3:n.135+5306C>A
ENST00000475622.5:c.135+5306C>A	ENSP00000423472.1:n.135+5306C>A
ENST00000514484.6:n.165+2943C>A
NM_024830.3:c.135+5306C>A	NP_079106.3:n.135+5306C>A
XM_005248373.2:c.-10+2943C>A	XP_005248430.1:n.-10+2943C>A
XM_011514133.1:c.201+7111C>A	XP_011512435.1:n.201+7111C>A
NM_024830.4:c.135+5306C>A	NP_079106.3:n.135+5306C>A
XM_005248373.3:c.-10+2943C>A	XP_005248430.1:n.-10+2943C>A
NM_024830.5:c.135+5306C>A MANE Select	NP_079106.3:n.135+5306C>A