Canonical Allele Identifier: CA400370338

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350959G>C (hg19) ; chr17:g.58273598G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273598G>C , CM000679.2:g.58273598G>C	GRCh38
NC_000017.10:g.56350959G>C , CM000679.1:g.56350959G>C	GRCh37
NC_000017.9:g.53705958G>C	NCBI36
NG_009629.1:g.12338C>G , LRG_84:g.12338C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.770C>G
ENST00000699291.1:c.562C>G	ENSP00000514272.1:p.Pro188Ala
ENST00000699292.1:n.477C>G
ENST00000225275.4:c.1437C>G MANE Select	ENSP00000225275.3:p.Tyr479Ter
ENST00000225275.3:c.1437C>G	ENSP00000225275.3:p.Tyr479Ter
NM_000250.1:c.1437C>G , LRG_84t1:c.1437C>G	NP_000241.1:p.Tyr479Ter
XM_011524821.1:c.1623C>G	XP_011523123.1:p.Tyr541Ter
XM_011524822.1:c.1152C>G	XP_011523124.1:p.Tyr384Ter
XM_011524823.1:c.1462C>G	XP_011523125.1:p.Pro488Ala
NM_000250.2:c.1437C>G MANE Select	NP_000241.1:p.Tyr479Ter