Canonical Allele Identifier: CA501023616

Gene: MPO

Linked Data

• COSMIC: COSM81428 ; COSM4947684
• MyVariant Identifiers: chr17:g.56351009G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273648G>A , CM000679.2:g.58273648G>A	GRCh38
NC_000017.10:g.56351009G>A , CM000679.1:g.56351009G>A	GRCh37
NC_000017.9:g.53706008G>A	NCBI36
NG_009629.1:g.12288C>T , LRG_84:g.12288C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.720C>T
ENST00000699291.1:c.512C>T	ENSP00000514272.1:p.Pro171Leu
ENST00000699292.1:n.427C>T
ENST00000225275.4:c.1387C>T MANE Select	ENSP00000225275.3:p.Leu463=
ENST00000225275.3:c.1387C>T	ENSP00000225275.3:p.Leu463=
NM_000250.1:c.1387C>T , LRG_84t1:c.1387C>T	NP_000241.1:p.Leu463=
XM_011524821.1:c.1573C>T	XP_011523123.1:p.Leu525=
XM_011524822.1:c.1102C>T	XP_011523124.1:p.Leu368=
XM_011524823.1:c.1412C>T	XP_011523125.1:p.Pro471Leu
NM_000250.2:c.1387C>T MANE Select	NP_000241.1:p.Leu463=