Canonical Allele Identifier: CA2638971641
Gene: MPO HGNC NCBI

Linked Data

gnomAD v4: 17-58273376-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58273376C>T , CM000679.2:g.58273376C>T GRCh38
NC_000017.10:g.56350737C>T , CM000679.1:g.56350737C>T GRCh37
NC_000017.9:g.53705736C>T NCBI36
NG_009629.1:g.12560G>A , LRG_84:g.12560G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000578493.2:n.954+38G>A
ENST00000699291.1:c.746+38G>A ENSP00000514272.1:n.746+38G>A
ENST00000699292.1:n.699G>A
ENST00000225275.4:c.1621+38G>A MANE Select ENSP00000225275.3:n.1621+38G>A
ENST00000225275.3:c.1621+38G>A ENSP00000225275.3:n.1621+38G>A
ENST00000577220.1:c.79+38G>A ENSP00000464668.1:n.79+38G>A
NM_000250.1:c.1621+38G>A , LRG_84t1:c.1621+38G>A NP_000241.1:n.1621+38G>A
XM_011524821.1:c.1807+38G>A XP_011523123.1:n.1807+38G>A
XM_011524822.1:c.1336+38G>A XP_011523124.1:n.1336+38G>A
NM_000250.2:c.1621+38G>A MANE Select NP_000241.1:n.1621+38G>A
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