Canonical Allele Identifier: CA1140177708

Gene: LPAR3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.84824726T= , CM000663.2:g.84824726T=	GRCh38
NC_000001.10:g.85290409T= , CM000663.1:g.85290409T=	GRCh37
NC_000001.9:g.85062997T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012152.3:c.737-10555A= MANE Select	NP_036284.1:n.737-10555A=
ENST00000370611.4:c.737-10555A= MANE Select	ENSP00000359643.3:n.737-10555A=
NM_012152.2:c.737-10555A=	NP_036284.1:n.737-10555A=
ENST00000370611.3:c.737-10555A=	ENSP00000359643.3:n.737-10555A=
ENST00000440886.1:c.737-10555A=	ENSP00000395389.1:n.737-10555A=
ENST00000491034.1:n.616-10555A=
XM_011541149.1:c.737-10555A=	XP_011539451.1:n.737-10555A=
XM_024446127.1:c.770-10555A=	XP_024301895.1:n.770-10555A=
XM_024446128.1:c.737-10555A=	XP_024301896.1:n.737-10555A=