Canonical Allele Identifier: CA501022311

Gene: MPO

Linked Data

• dbSNP Id: rs1287202897
• gnomAD v2: 17-56350824-A-G
• gnomAD v4: 17-58273463-A-G
• MyVariant Identifiers: chr17:g.56350824A>G (hg19) ; chr17:g.58273463A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273463A>G , CM000679.2:g.58273463A>G	GRCh38
NC_000017.10:g.56350824A>G , CM000679.1:g.56350824A>G	GRCh37
NC_000017.9:g.53705823A>G	NCBI36
NG_009629.1:g.12473T>C , LRG_84:g.12473T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.905T>C
ENST00000699291.1:c.697T>C	ENSP00000514272.1:n.697T>C
ENST00000699292.1:n.612T>C
ENST00000225275.4:c.1572T>C MANE Select	ENSP00000225275.3:p.Arg524=
ENST00000225275.3:c.1572T>C	ENSP00000225275.3:p.Arg524=
ENST00000577220.1:c.30T>C	ENSP00000464668.1:p.Arg10=
NM_000250.1:c.1572T>C , LRG_84t1:c.1572T>C	NP_000241.1:p.Arg524=
XM_011524821.1:c.1758T>C	XP_011523123.1:p.Arg586=
XM_011524822.1:c.1287T>C	XP_011523124.1:p.Arg429=
XM_011524823.1:c.*121T>C	XP_011523125.1:n.*121T>C
NM_000250.2:c.1572T>C MANE Select	NP_000241.1:p.Arg524=