Canonical Allele Identifier: CA400369991

Gene: MPO

Linked Data

• gnomAD v4: 17-58273509-A-G
• MyVariant Identifiers: chr17:g.56350870A>G (hg19) ; chr17:g.58273509A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273509A>G , CM000679.2:g.58273509A>G	GRCh38
NC_000017.10:g.56350870A>G , CM000679.1:g.56350870A>G	GRCh37
NC_000017.9:g.53705869A>G	NCBI36
NG_009629.1:g.12427T>C , LRG_84:g.12427T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.859T>C
ENST00000699291.1:c.651T>C	ENSP00000514272.1:n.651T>C
ENST00000699292.1:n.566T>C
ENST00000225275.4:c.1526T>C MANE Select	ENSP00000225275.3:p.Met509Thr
ENST00000225275.3:c.1526T>C	ENSP00000225275.3:p.Met509Thr
NM_000250.1:c.1526T>C , LRG_84t1:c.1526T>C	NP_000241.1:p.Met509Thr
XM_011524821.1:c.1712T>C	XP_011523123.1:p.Met571Thr
XM_011524822.1:c.1241T>C	XP_011523124.1:p.Met414Thr
XM_011524823.1:c.*75T>C	XP_011523125.1:n.*75T>C
NM_000250.2:c.1526T>C MANE Select	NP_000241.1:p.Met509Thr