Canonical Allele Identifier: CA2638975871
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280913-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280915del , CM000679.2:g.58280915del GRCh38
NC_000017.10:g.56358276del , CM000679.1:g.56358276del GRCh37
NC_000017.9:g.53713275del NCBI36
NG_009629.1:g.5022del , LRG_84:g.5022del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-156del MANE Select ENSP00000225275.3:n.-156del
ENST00000225275.3:c.-156del ENSP00000225275.3:n.-156del
NM_000250.1:c.-156del , LRG_84t1:c.-156del NP_000241.1:n.-156del
XM_011524821.1:c.215+11del XP_011523123.1:n.215+11del
XM_011524823.1:c.215+11del XP_011523125.1:n.215+11del
NM_000250.2:c.-156del MANE Select NP_000241.1:n.-156del
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