Canonical Allele Identifier: CA400370431

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350985C>A (hg19) ; chr17:g.58273624C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273624C>A , CM000679.2:g.58273624C>A	GRCh38
NC_000017.10:g.56350985C>A , CM000679.1:g.56350985C>A	GRCh37
NC_000017.9:g.53705984C>A	NCBI36
NG_009629.1:g.12312G>T , LRG_84:g.12312G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.744G>T
ENST00000699291.1:c.536G>T	ENSP00000514272.1:p.Gly179Val
ENST00000699292.1:n.451G>T
ENST00000225275.4:c.1411G>T MANE Select	ENSP00000225275.3:p.Ala471Ser
ENST00000225275.3:c.1411G>T	ENSP00000225275.3:p.Ala471Ser
NM_000250.1:c.1411G>T , LRG_84t1:c.1411G>T	NP_000241.1:p.Ala471Ser
XM_011524821.1:c.1597G>T	XP_011523123.1:p.Ala533Ser
XM_011524822.1:c.1126G>T	XP_011523124.1:p.Ala376Ser
XM_011524823.1:c.1436G>T	XP_011523125.1:p.Gly479Val
NM_000250.2:c.1411G>T MANE Select	NP_000241.1:p.Ala471Ser