Canonical Allele Identifier: CA773481932

Gene: MPO

Linked Data

• dbSNP Id: rs1396494429
• MyVariant Identifiers: chr17:g.56351019_56351022del (hg19) ; chr17:g.58273658_58273661del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273660_58273663del , CM000679.2:g.58273660_58273663del	GRCh38
NC_000017.10:g.56351021_56351024del , CM000679.1:g.56351021_56351024del	GRCh37
NC_000017.9:g.53706020_53706023del	NCBI36
NG_009629.1:g.12275_12278del , LRG_84:g.12275_12278del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.707_710del
ENST00000699291.1:c.499_502del	ENSP00000514272.1:p.Leu167ArgfsTer?
ENST00000699292.1:n.414_417del
ENST00000225275.4:c.1374_1377del MANE Select	ENSP00000225275.3:p.Tyr459GlyfsTer13
ENST00000225275.3:c.1374_1377del	ENSP00000225275.3:p.Tyr459GlyfsTer13
NM_000250.1:c.1374_1377del , LRG_84t1:c.1374_1377del	NP_000241.1:p.Tyr459GlyfsTer13
XM_011524821.1:c.1560_1563del	XP_011523123.1:p.Tyr521GlyfsTer13
XM_011524822.1:c.1089_1092del	XP_011523124.1:p.Tyr364GlyfsTer13
XM_011524823.1:c.1399_1402del	XP_011523125.1:p.Leu467ArgfsTer?
NM_000250.2:c.1374_1377del MANE Select	NP_000241.1:p.Tyr459GlyfsTer13