Canonical Allele Identifier: CA400369997

Gene: MPO

Linked Data

• dbSNP Id: rs1381469903
• MyVariant Identifiers: chr17:g.56350871T>G (hg19) ; chr17:g.58273510T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273510T>G , CM000679.2:g.58273510T>G	GRCh38
NC_000017.10:g.56350871T>G , CM000679.1:g.56350871T>G	GRCh37
NC_000017.9:g.53705870T>G	NCBI36
NG_009629.1:g.12426A>C , LRG_84:g.12426A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.858A>C
ENST00000699291.1:c.650A>C	ENSP00000514272.1:n.650A>C
ENST00000699292.1:n.565A>C
ENST00000225275.4:c.1525A>C MANE Select	ENSP00000225275.3:p.Met509Leu
ENST00000225275.3:c.1525A>C	ENSP00000225275.3:p.Met509Leu
NM_000250.1:c.1525A>C , LRG_84t1:c.1525A>C	NP_000241.1:p.Met509Leu
XM_011524821.1:c.1711A>C	XP_011523123.1:p.Met571Leu
XM_011524822.1:c.1240A>C	XP_011523124.1:p.Met414Leu
XM_011524823.1:c.*74A>C	XP_011523125.1:n.*74A>C
NM_000250.2:c.1525A>C MANE Select	NP_000241.1:p.Met509Leu