Canonical Allele Identifier: CA5522633
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2881546
ClinVar RCV Id: RCV003742501
dbSNP Id: rs764740119

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166343C>T , CM000672.2:g.68166343C>T GRCh38
NC_000010.10:g.69926100C>T , CM000672.1:g.69926100C>T GRCh37
NC_000010.9:g.69596106C>T NCBI36
NG_032118.1:g.65227C>T , LRG_410:g.65227C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.825C>T ENSP00000346369.2:p.Thr275=
ENST00000373675.4:c.1650C>T ENSP00000362779.4:p.Thr550=
ENST00000540630.6:c.1704C>T ENSP00000441668.3:p.Thr568=
ENST00000613327.5:c.1650C>T ENSP00000480757.2:p.Thr550=
ENST00000687572.1:c.528C>T ENSP00000510427.1:p.Thr176=
ENST00000687705.1:c.*1899C>T ENSP00000509639.1:n.*1899C>T
ENST00000688812.1:c.1626C>T ENSP00000510658.1:p.Thr542=
ENST00000689002.1:n.702C>T
ENST00000690544.1:c.*921C>T ENSP00000508989.1:n.*921C>T
ENST00000358913.10:c.1650C>T MANE Select ENSP00000351790.5:p.Thr550=
ENST00000354393.6:c.825C>T ENSP00000346369.2:p.Thr275=
ENST00000358913.9:c.1650C>T ENSP00000351790.5:p.Thr550=
ENST00000540630.5:c.1650C>T ENSP00000441668.2:p.Thr550=
ENST00000613327.4:c.768C>T ENSP00000480757.1:p.Thr256=
NM_001256267.1:c.1650C>T NP_001243196.1:p.Thr550=
NM_001256268.1:c.768C>T NP_001243197.1:p.Thr256=
NM_032578.3:c.1650C>T , LRG_410t1:c.1650C>T NP_115967.2:p.Thr550=
NR_045662.3:n.1077C>T
NR_045663.3:n.1918C>T
XM_006718043.2:c.1704C>T XP_006718106.1:p.Thr568=
XM_011540292.1:c.1680C>T XP_011538594.1:p.Thr560=
XM_017016833.1:c.1728C>T XP_016872322.1:p.Thr576=
XM_017016834.2:c.1650C>T XP_016872323.1:p.Thr550=
XM_024448236.1:c.528C>T XP_024304004.1:p.Thr176=
NR_045662.4:n.1187C>T
NR_045663.4:n.1863C>T
NM_001256267.2:c.1650C>T NP_001243196.1:p.Thr550=
NM_001256268.2:c.768C>T NP_001243197.1:p.Thr256=
NM_032578.4:c.1650C>T MANE Select NP_115967.2:p.Thr550=