Canonical Allele Identifier: CA400370267

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350939A>G (hg19) ; chr17:g.58273578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273578A>G , CM000679.2:g.58273578A>G	GRCh38
NC_000017.10:g.56350939A>G , CM000679.1:g.56350939A>G	GRCh37
NC_000017.9:g.53705938A>G	NCBI36
NG_009629.1:g.12358T>C , LRG_84:g.12358T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.790T>C
ENST00000699291.1:c.582T>C	ENSP00000514272.1:n.582T>C
ENST00000699292.1:n.497T>C
ENST00000225275.4:c.1457T>C MANE Select	ENSP00000225275.3:p.Val486Ala
ENST00000225275.3:c.1457T>C	ENSP00000225275.3:p.Val486Ala
NM_000250.1:c.1457T>C , LRG_84t1:c.1457T>C	NP_000241.1:p.Val486Ala
XM_011524821.1:c.1643T>C	XP_011523123.1:p.Val548Ala
XM_011524822.1:c.1172T>C	XP_011523124.1:p.Val391Ala
XM_011524823.1:c.*6T>C	XP_011523125.1:n.*6T>C
NM_000250.2:c.1457T>C MANE Select	NP_000241.1:p.Val486Ala