Canonical Allele Identifier: CA2832558042
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199387dup , CM000672.2:g.68199387dup GRCh38
NC_000010.10:g.69959144dup , CM000672.1:g.69959144dup GRCh37
NC_000010.9:g.69629150dup NCBI36
NG_032118.1:g.98271dup , LRG_410:g.98271dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2480dup ENSP00000346369.2:p.Glu828GlyfsTer?
ENST00000540630.6:c.3359dup ENSP00000441668.3:p.Glu1121GlyfsTer?
ENST00000613327.5:c.3305dup ENSP00000480757.2:p.Glu1103GlyfsTer?
ENST00000688812.1:c.*568dup ENSP00000510658.1:n.*568dup
ENST00000690544.1:c.*2576dup ENSP00000508989.1:n.*2576dup
ENST00000358913.10:c.3305dup MANE Select ENSP00000351790.5:p.Glu1103GlyfsTer?
ENST00000354393.6:c.2480dup ENSP00000346369.2:p.Glu828GlyfsTer?
ENST00000358913.9:c.3305dup ENSP00000351790.5:p.Glu1103GlyfsTer?
ENST00000540630.5:c.3305dup ENSP00000441668.2:p.Glu1103GlyfsTer?
ENST00000613327.4:c.2423dup ENSP00000480757.1:p.Glu809GlyfsTer?
NM_001256267.1:c.3305dup NP_001243196.1:p.Glu1103GlyfsTer?
NM_001256268.1:c.2423dup NP_001243197.1:p.Glu809GlyfsTer?
NM_032578.3:c.3305dup , LRG_410t1:c.3305dup NP_115967.2:p.Glu1103GlyfsTer?
NR_045662.3:n.2732dup
NR_045663.3:n.3434dup
XM_006718043.2:c.3359dup XP_006718106.1:p.Glu1121GlyfsTer?
XM_011540292.1:c.3335dup XP_011538594.1:p.Glu1113GlyfsTer?
XR_946029.1:n.1804-108dup
XM_017016833.1:c.3383dup XP_016872322.1:p.Glu1129GlyfsTer?
XM_017016834.2:c.3305dup XP_016872323.1:p.Glu1103GlyfsTer?
XM_024448236.1:c.2183dup XP_024304004.1:p.Glu729GlyfsTer?
NR_045662.4:n.2842dup
NR_045663.4:n.3379dup
NM_001256267.2:c.3305dup NP_001243196.1:p.Glu1103GlyfsTer?
NM_001256268.2:c.2423dup NP_001243197.1:p.Glu809GlyfsTer?
NM_032578.4:c.3305dup MANE Select NP_115967.2:p.Glu1103GlyfsTer?