Canonical Allele Identifier: CA2576333135
Gene: MPO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58279460G>T , CM000679.2:g.58279460G>T GRCh38
NC_000017.10:g.56356821G>T , CM000679.1:g.56356821G>T GRCh37
NC_000017.9:g.53711820G>T NCBI36
NG_009629.1:g.6476C>A , LRG_84:g.6476C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.549-34C>A MANE Select ENSP00000225275.3:n.549-34C>A
ENST00000225275.3:c.549-34C>A ENSP00000225275.3:n.549-34C>A
NM_000250.1:c.549-34C>A , LRG_84t1:c.549-34C>A NP_000241.1:n.549-34C>A
XM_011524821.1:c.735-34C>A XP_011523123.1:n.735-34C>A
XM_011524822.1:c.264-34C>A XP_011523124.1:n.264-34C>A
XM_011524823.1:c.735-34C>A XP_011523125.1:n.735-34C>A
NM_000250.2:c.549-34C>A MANE Select NP_000241.1:n.549-34C>A
Search 100 bp 5'
Search 100 bp 3'