Canonical Allele Identifier: CA400370415

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350980C>G (hg19) ; chr17:g.58273619C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273619C>G , CM000679.2:g.58273619C>G	GRCh38
NC_000017.10:g.56350980C>G , CM000679.1:g.56350980C>G	GRCh37
NC_000017.9:g.53705979C>G	NCBI36
NG_009629.1:g.12317G>C , LRG_84:g.12317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.749G>C
ENST00000699291.1:c.541G>C	ENSP00000514272.1:p.Glu181Gln
ENST00000699292.1:n.456G>C
ENST00000225275.4:c.1416G>C MANE Select	ENSP00000225275.3:p.Met472Ile
ENST00000225275.3:c.1416G>C	ENSP00000225275.3:p.Met472Ile
NM_000250.1:c.1416G>C , LRG_84t1:c.1416G>C	NP_000241.1:p.Met472Ile
XM_011524821.1:c.1602G>C	XP_011523123.1:p.Met534Ile
XM_011524822.1:c.1131G>C	XP_011523124.1:p.Met377Ile
XM_011524823.1:c.1441G>C	XP_011523125.1:p.Glu481Gln
NM_000250.2:c.1416G>C MANE Select	NP_000241.1:p.Met472Ile