Canonical Allele Identifier: CA2638975002
Gene: MPO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58280358T>C , CM000679.2:g.58280358T>C GRCh38
NC_000017.10:g.56357719T>C , CM000679.1:g.56357719T>C GRCh37
NC_000017.9:g.53712718T>C NCBI36
NG_009629.1:g.5578A>G , LRG_84:g.5578A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225275.4:c.248+8A>G MANE Select ENSP00000225275.3:n.248+8A>G
ENST00000225275.3:c.248+8A>G ENSP00000225275.3:n.248+8A>G
ENST00000580005.1:n.185A>G
NM_000250.1:c.248+8A>G , LRG_84t1:c.248+8A>G NP_000241.1:n.248+8A>G
XM_011524821.1:c.434+8A>G XP_011523123.1:n.434+8A>G
XM_011524822.1:c.-38+247A>G XP_011523124.1:n.-38+247A>G
XM_011524823.1:c.434+8A>G XP_011523125.1:n.434+8A>G
NM_000250.2:c.248+8A>G MANE Select NP_000241.1:n.248+8A>G