Canonical Allele Identifier: CA400368978

Gene: MPO

Linked Data

• dbSNP Id: rs774984207
• gnomAD v2: 17-56350118-C-A
• MyVariant Identifiers: chr17:g.56350118C>A (hg19) ; chr17:g.58272757C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58272757C>A , CM000679.2:g.58272757C>A	GRCh38
NC_000017.10:g.56350118C>A , CM000679.1:g.56350118C>A	GRCh37
NC_000017.9:g.53705117C>A	NCBI36
NG_009629.1:g.13179G>T , LRG_84:g.13179G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578493.2:n.1116G>T
ENST00000699291.1:c.908G>T	ENSP00000514272.1:n.908G>T
ENST00000699292.1:n.1318G>T
ENST00000225275.4:c.1783G>T MANE Select	ENSP00000225275.3:p.Gly595Cys
ENST00000225275.3:c.1783G>T	ENSP00000225275.3:p.Gly595Cys
ENST00000577220.1:c.183+58G>T	ENSP00000464668.1:n.183+58G>T
NM_000250.1:c.1783G>T , LRG_84t1:c.1783G>T	NP_000241.1:p.Gly595Cys
XM_011524821.1:c.1969G>T	XP_011523123.1:p.Gly657Cys
XM_011524822.1:c.1498G>T	XP_011523124.1:p.Gly500Cys
NM_000250.2:c.1783G>T MANE Select	NP_000241.1:p.Gly595Cys