Canonical Allele Identifier: CA501321919
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56357732C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280371C>T , CM000679.2:g.58280371C>T GRCh38
NC_000017.10:g.56357732C>T , CM000679.1:g.56357732C>T GRCh37
NC_000017.9:g.53712731C>T NCBI36
NG_009629.1:g.5565G>A , LRG_84:g.5565G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.243G>A MANE Select ENSP00000225275.3:p.Arg81=
ENST00000225275.3:c.243G>A ENSP00000225275.3:p.Arg81=
ENST00000580005.1:n.172G>A
NM_000250.1:c.243G>A , LRG_84t1:c.243G>A NP_000241.1:p.Arg81=
XM_011524821.1:c.429G>A XP_011523123.1:p.Arg143=
XM_011524822.1:c.-38+234G>A XP_011523124.1:n.-38+234G>A
XM_011524823.1:c.429G>A XP_011523125.1:p.Arg143=
NM_000250.2:c.243G>A MANE Select NP_000241.1:p.Arg81=