Canonical Allele Identifier: CA400370437

Gene: MPO

Linked Data

• gnomAD v4: 17-58273626-G-C
• MyVariant Identifiers: chr17:g.56350987G>C (hg19) ; chr17:g.58273626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273626G>C , CM000679.2:g.58273626G>C	GRCh38
NC_000017.10:g.56350987G>C , CM000679.1:g.56350987G>C	GRCh37
NC_000017.9:g.53705986G>C	NCBI36
NG_009629.1:g.12310C>G , LRG_84:g.12310C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.742C>G
ENST00000699291.1:c.534C>G	ENSP00000514272.1:p.Asn178Lys
ENST00000699292.1:n.449C>G
ENST00000225275.4:c.1409C>G MANE Select	ENSP00000225275.3:p.Thr470Arg
ENST00000225275.3:c.1409C>G	ENSP00000225275.3:p.Thr470Arg
NM_000250.1:c.1409C>G , LRG_84t1:c.1409C>G	NP_000241.1:p.Thr470Arg
XM_011524821.1:c.1595C>G	XP_011523123.1:p.Thr532Arg
XM_011524822.1:c.1124C>G	XP_011523124.1:p.Thr375Arg
XM_011524823.1:c.1434C>G	XP_011523125.1:p.Asn478Lys
NM_000250.2:c.1409C>G MANE Select	NP_000241.1:p.Thr470Arg