Canonical Allele Identifier: CA400370280

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350943A>C (hg19) ; chr17:g.58273582A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273582A>C , CM000679.2:g.58273582A>C	GRCh38
NC_000017.10:g.56350943A>C , CM000679.1:g.56350943A>C	GRCh37
NC_000017.9:g.53705942A>C	NCBI36
NG_009629.1:g.12354T>G , LRG_84:g.12354T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.786T>G
ENST00000699291.1:c.578T>G	ENSP00000514272.1:n.578T>G
ENST00000699292.1:n.493T>G
ENST00000225275.4:c.1453T>G MANE Select	ENSP00000225275.3:p.Ser485Ala
ENST00000225275.3:c.1453T>G	ENSP00000225275.3:p.Ser485Ala
NM_000250.1:c.1453T>G , LRG_84t1:c.1453T>G	NP_000241.1:p.Ser485Ala
XM_011524821.1:c.1639T>G	XP_011523123.1:p.Ser547Ala
XM_011524822.1:c.1168T>G	XP_011523124.1:p.Ser390Ala
XM_011524823.1:c.*2T>G	XP_011523125.1:n.*2T>G
NM_000250.2:c.1453T>G MANE Select	NP_000241.1:p.Ser485Ala