Canonical Allele Identifier: CA14407357

Gene: LPO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58267082T>C , CM000679.2:g.58267082T>C	GRCh38
NC_000017.10:g.56344443T>C , CM000679.1:g.56344443T>C	GRCh37
NC_000017.9:g.53699442T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262290.9:c.1694-267T>C MANE Select	ENSP00000262290.4:n.1694-267T>C
ENST00000262290.8:c.1694-267T>C	ENSP00000262290.4:n.1694-267T>C
ENST00000389576.4:c.973-267T>C	ENSP00000374227.4:n.973-267T>C
ENST00000421678.6:c.1445-267T>C	ENSP00000400245.2:n.1445-267T>C
ENST00000543544.5:c.1517-267T>C	ENSP00000445344.1:n.1517-267T>C
ENST00000580890.5:c.1081-267T>C	ENSP00000462752.1:n.1081-267T>C
ENST00000582328.5:c.1445-267T>C	ENSP00000464636.1:n.1445-267T>C
NM_001160102.1:c.1445-267T>C	NP_001153574.1:n.1445-267T>C
NM_006151.2:c.1694-267T>C	NP_006142.1:n.1694-267T>C
NR_027647.1:n.1922-267T>C
XM_011524808.1:c.1280-267T>C	XP_011523110.1:n.1280-267T>C
XM_011524809.1:c.1043-267T>C	XP_011523111.1:n.1043-267T>C
XM_011524810.1:c.935-267T>C	XP_011523112.1:n.935-267T>C
XM_011524808.2:c.1280-267T>C	XP_011523110.1:n.1280-267T>C
XM_011524810.2:c.935-267T>C	XP_011523112.1:n.935-267T>C
NM_006151.3:c.1694-267T>C MANE Select	NP_006142.1:n.1694-267T>C
NR_027647.2:n.1764-267T>C
NM_001160102.2:c.1445-267T>C	NP_001153574.1:n.1445-267T>C