Canonical Allele Identifier: CA400370173

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350909T>C (hg19) ; chr17:g.58273548T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273548T>C , CM000679.2:g.58273548T>C	GRCh38
NC_000017.10:g.56350909T>C , CM000679.1:g.56350909T>C	GRCh37
NC_000017.9:g.53705908T>C	NCBI36
NG_009629.1:g.12388A>G , LRG_84:g.12388A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.820A>G
ENST00000699291.1:c.612A>G	ENSP00000514272.1:n.612A>G
ENST00000699292.1:n.527A>G
ENST00000225275.4:c.1487A>G MANE Select	ENSP00000225275.3:p.Asn496Ser
ENST00000225275.3:c.1487A>G	ENSP00000225275.3:p.Asn496Ser
NM_000250.1:c.1487A>G , LRG_84t1:c.1487A>G	NP_000241.1:p.Asn496Ser
XM_011524821.1:c.1673A>G	XP_011523123.1:p.Asn558Ser
XM_011524822.1:c.1202A>G	XP_011523124.1:p.Asn401Ser
XM_011524823.1:c.*36A>G	XP_011523125.1:n.*36A>G
NM_000250.2:c.1487A>G MANE Select	NP_000241.1:p.Asn496Ser