Canonical Allele Identifier: CA400370158

Gene: MPO

Linked Data

• gnomAD v4: 17-58273545-G-A
• MyVariant Identifiers: chr17:g.56350906G>A (hg19) ; chr17:g.58273545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273545G>A , CM000679.2:g.58273545G>A	GRCh38
NC_000017.10:g.56350906G>A , CM000679.1:g.56350906G>A	GRCh37
NC_000017.9:g.53705905G>A	NCBI36
NG_009629.1:g.12391C>T , LRG_84:g.12391C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.823C>T
ENST00000699291.1:c.615C>T	ENSP00000514272.1:n.615C>T
ENST00000699292.1:n.530C>T
ENST00000225275.4:c.1490C>T MANE Select	ENSP00000225275.3:p.Ala497Val
ENST00000225275.3:c.1490C>T	ENSP00000225275.3:p.Ala497Val
NM_000250.1:c.1490C>T , LRG_84t1:c.1490C>T	NP_000241.1:p.Ala497Val
XM_011524821.1:c.1676C>T	XP_011523123.1:p.Ala559Val
XM_011524822.1:c.1205C>T	XP_011523124.1:p.Ala402Val
XM_011524823.1:c.*39C>T	XP_011523125.1:n.*39C>T
NM_000250.2:c.1490C>T MANE Select	NP_000241.1:p.Ala497Val