Canonical Allele Identifier: CA2528952126
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280520G>T , CM000679.2:g.58280520G>T GRCh38
NC_000017.10:g.56357881G>T , CM000679.1:g.56357881G>T GRCh37
NC_000017.9:g.53712880G>T NCBI36
NG_009629.1:g.5416C>A , LRG_84:g.5416C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.155-61C>A MANE Select ENSP00000225275.3:n.155-61C>A
ENST00000225275.3:c.155-61C>A ENSP00000225275.3:n.155-61C>A
ENST00000580005.1:n.84-61C>A
NM_000250.1:c.155-61C>A , LRG_84t1:c.155-61C>A NP_000241.1:n.155-61C>A
XM_011524821.1:c.341-61C>A XP_011523123.1:n.341-61C>A
XM_011524822.1:c.-38+85C>A XP_011523124.1:n.-38+85C>A
XM_011524823.1:c.341-61C>A XP_011523125.1:n.341-61C>A
NM_000250.2:c.155-61C>A MANE Select NP_000241.1:n.155-61C>A
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