Canonical Allele Identifier: CA400369594

Gene: MPO

Linked Data

• gnomAD v4: 17-58273414-C-T
• MyVariant Identifiers: chr17:g.56350775C>T (hg19) ; chr17:g.58273414C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273414C>T , CM000679.2:g.58273414C>T	GRCh38
NC_000017.10:g.56350775C>T , CM000679.1:g.56350775C>T	GRCh37
NC_000017.9:g.53705774C>T	NCBI36
NG_009629.1:g.12522G>A , LRG_84:g.12522G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.954G>A
ENST00000699291.1:c.746G>A	ENSP00000514272.1:n.746G>A
ENST00000699292.1:n.661G>A
ENST00000225275.4:c.1621G>A MANE Select	ENSP00000225275.3:p.Gly541Ser
ENST00000225275.3:c.1621G>A	ENSP00000225275.3:p.Gly541Ser
ENST00000577220.1:c.79G>A	ENSP00000464668.1:p.Gly27Ser
NM_000250.1:c.1621G>A , LRG_84t1:c.1621G>A	NP_000241.1:p.Gly541Ser
XM_011524821.1:c.1807G>A	XP_011523123.1:p.Gly603Ser
XM_011524822.1:c.1336G>A	XP_011523124.1:p.Gly446Ser
NM_000250.2:c.1621G>A MANE Select	NP_000241.1:p.Gly541Ser