Canonical Allele Identifier: CA501321988
Gene: MPO HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.56357759C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280398C>A , CM000679.2:g.58280398C>A GRCh38
NC_000017.10:g.56357759C>A , CM000679.1:g.56357759C>A GRCh37
NC_000017.9:g.53712758C>A NCBI36
NG_009629.1:g.5538G>T , LRG_84:g.5538G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225275.4:c.216G>T MANE Select ENSP00000225275.3:p.Leu72=
ENST00000225275.3:c.216G>T ENSP00000225275.3:p.Leu72=
ENST00000580005.1:n.145G>T
NM_000250.1:c.216G>T , LRG_84t1:c.216G>T NP_000241.1:p.Leu72=
XM_011524821.1:c.402G>T XP_011523123.1:p.Leu134=
XM_011524822.1:c.-38+207G>T XP_011523124.1:n.-38+207G>T
XM_011524823.1:c.402G>T XP_011523125.1:p.Leu134=
NM_000250.2:c.216G>T MANE Select NP_000241.1:p.Leu72=