Canonical Allele Identifier: CA400370466

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350996A>G (hg19) ; chr17:g.58273635A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273635A>G , CM000679.2:g.58273635A>G	GRCh38
NC_000017.10:g.56350996A>G , CM000679.1:g.56350996A>G	GRCh37
NC_000017.9:g.53705995A>G	NCBI36
NG_009629.1:g.12301T>C , LRG_84:g.12301T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.733T>C
ENST00000699291.1:c.525T>C	ENSP00000514272.1:p.Ala175=
ENST00000699292.1:n.440T>C
ENST00000225275.4:c.1400T>C MANE Select	ENSP00000225275.3:p.Leu467Pro
ENST00000225275.3:c.1400T>C	ENSP00000225275.3:p.Leu467Pro
NM_000250.1:c.1400T>C , LRG_84t1:c.1400T>C	NP_000241.1:p.Leu467Pro
XM_011524821.1:c.1586T>C	XP_011523123.1:p.Leu529Pro
XM_011524822.1:c.1115T>C	XP_011523124.1:p.Leu372Pro
XM_011524823.1:c.1425T>C	XP_011523125.1:p.Ala475=
NM_000250.2:c.1400T>C MANE Select	NP_000241.1:p.Leu467Pro