Canonical Allele Identifier: CA400370433

Gene: MPO

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.744G>C
ENST00000699291.1:c.536G>C	ENSP00000514272.1:p.Gly179Ala
ENST00000699292.1:n.451G>C
ENST00000225275.4:c.1411G>C MANE Select	ENSP00000225275.3:p.Ala471Pro
ENST00000225275.3:c.1411G>C	ENSP00000225275.3:p.Ala471Pro
NM_000250.1:c.1411G>C , LRG_84t1:c.1411G>C	NP_000241.1:p.Ala471Pro
XM_011524821.1:c.1597G>C	XP_011523123.1:p.Ala533Pro
XM_011524822.1:c.1126G>C	XP_011523124.1:p.Ala376Pro
XM_011524823.1:c.1436G>C	XP_011523125.1:p.Gly479Ala
NM_000250.2:c.1411G>C MANE Select	NP_000241.1:p.Ala471Pro