Canonical Allele Identifier: CA1139906644

Gene: LPAR3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84845509C= , CM000663.2:g.84845509C=	GRCh38
NC_000001.10:g.85311192C= , CM000663.1:g.85311192C=	GRCh37
NC_000001.9:g.85083780C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370611.4:c.736+19876G= MANE Select	ENSP00000359643.3:n.736+19876G=
ENST00000370611.3:c.736+19876G=	ENSP00000359643.3:n.736+19876G=
ENST00000440886.1:c.736+19876G=	ENSP00000395389.1:n.736+19876G=
ENST00000491034.1:n.615+19876G=
NM_012152.2:c.736+19876G=	NP_036284.1:n.736+19876G=
XM_011541149.1:c.736+19876G=	XP_011539451.1:n.736+19876G=
XM_024446127.1:c.769+19876G=	XP_024301895.1:n.769+19876G=
XM_024446128.1:c.736+19876G=	XP_024301896.1:n.736+19876G=
NM_012152.3:c.736+19876G= MANE Select	NP_036284.1:n.736+19876G=