Canonical Allele Identifier: CA400370309

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56350950G>C (hg19) ; chr17:g.58273589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273589G>C , CM000679.2:g.58273589G>C	GRCh38
NC_000017.10:g.56350950G>C , CM000679.1:g.56350950G>C	GRCh37
NC_000017.9:g.53705949G>C	NCBI36
NG_009629.1:g.12347C>G , LRG_84:g.12347C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.779C>G
ENST00000699291.1:c.571C>G	ENSP00000514272.1:p.Gln191Glu
ENST00000699292.1:n.486C>G
ENST00000225275.4:c.1446C>G MANE Select	ENSP00000225275.3:p.Tyr482Ter
ENST00000225275.3:c.1446C>G	ENSP00000225275.3:p.Tyr482Ter
NM_000250.1:c.1446C>G , LRG_84t1:c.1446C>G	NP_000241.1:p.Tyr482Ter
XM_011524821.1:c.1632C>G	XP_011523123.1:p.Tyr544Ter
XM_011524822.1:c.1161C>G	XP_011523124.1:p.Tyr387Ter
XM_011524823.1:c.1471C>G	XP_011523125.1:p.Gln491Glu
NM_000250.2:c.1446C>G MANE Select	NP_000241.1:p.Tyr482Ter