Canonical Allele Identifier: CA400370501

Gene: MPO

Linked Data

• gnomAD v4: 17-58273648-G-T
• MyVariant Identifiers: chr17:g.56351009G>T (hg19) ; chr17:g.58273648G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273648G>T , CM000679.2:g.58273648G>T	GRCh38
NC_000017.10:g.56351009G>T , CM000679.1:g.56351009G>T	GRCh37
NC_000017.9:g.53706008G>T	NCBI36
NG_009629.1:g.12288C>A , LRG_84:g.12288C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.720C>A
ENST00000699291.1:c.512C>A	ENSP00000514272.1:p.Pro171His
ENST00000699292.1:n.427C>A
ENST00000225275.4:c.1387C>A MANE Select	ENSP00000225275.3:p.Leu463Met
ENST00000225275.3:c.1387C>A	ENSP00000225275.3:p.Leu463Met
NM_000250.1:c.1387C>A , LRG_84t1:c.1387C>A	NP_000241.1:p.Leu463Met
XM_011524821.1:c.1573C>A	XP_011523123.1:p.Leu525Met
XM_011524822.1:c.1102C>A	XP_011523124.1:p.Leu368Met
XM_011524823.1:c.1412C>A	XP_011523125.1:p.Pro471His
NM_000250.2:c.1387C>A MANE Select	NP_000241.1:p.Leu463Met