Canonical Allele Identifier: CA2638975862
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58280905-AC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280909del , CM000679.2:g.58280909del GRCh38
NC_000017.10:g.56358270del , CM000679.1:g.56358270del GRCh37
NC_000017.9:g.53713269del NCBI36
NG_009629.1:g.5030del , LRG_84:g.5030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.-148del MANE Select ENSP00000225275.3:n.-148del
ENST00000225275.3:c.-148del ENSP00000225275.3:n.-148del
NM_000250.1:c.-148del , LRG_84t1:c.-148del NP_000241.1:n.-148del
XM_011524821.1:c.215+19del XP_011523123.1:n.215+19del
XM_011524823.1:c.215+19del XP_011523125.1:n.215+19del
NM_000250.2:c.-148del MANE Select NP_000241.1:n.-148del
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