Canonical Allele Identifier: CA913191255

Gene: LPCAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55519320G>A , CM000678.2:g.55519320G>A	GRCh38
NC_000016.9:g.55553232G>A , CM000678.1:g.55553232G>A	GRCh37
NC_000016.8:g.54110733G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017839.5:c.172-6188G>A MANE Select	NP_060309.2:n.172-6188G>A
ENST00000262134.10:c.172-6188G>A MANE Select	ENSP00000262134.5:n.172-6188G>A
NM_017839.4:c.172-6188G>A	NP_060309.2:n.172-6188G>A
ENST00000262134.9:c.172-6188G>A	ENSP00000262134.5:n.172-6188G>A
ENST00000566911.1:n.282-6188G>A
XM_005256006.2:c.172-6188G>A	XP_005256063.1:n.172-6188G>A
XM_005256006.3:c.172-6188G>A	XP_005256063.1:n.172-6188G>A
XM_011523169.3:c.-621-6188G>A	XP_011521471.1:n.-621-6188G>A
XM_017023376.1:c.-56-244G>A	XP_016878865.1:n.-56-244G>A