Canonical Allele Identifier: CA5522605
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 227715
dbSNP Id: rs569718340

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68165754C>T , CM000672.2:g.68165754C>T GRCh38
NC_000010.10:g.69925511C>T , CM000672.1:g.69925511C>T GRCh37
NC_000010.9:g.69595517C>T NCBI36
NG_032118.1:g.64638C>T , LRG_410:g.64638C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.711C>T ENSP00000346369.2:p.Cys237=
ENST00000373675.4:c.1536C>T ENSP00000362779.4:p.Cys512=
ENST00000540630.6:c.1590C>T ENSP00000441668.3:p.Cys530=
ENST00000613327.5:c.1536C>T ENSP00000480757.2:p.Cys512=
ENST00000687572.1:c.414C>T ENSP00000510427.1:p.Cys138=
ENST00000687705.1:c.*1785C>T ENSP00000509639.1:n.*1785C>T
ENST00000688812.1:c.1512C>T ENSP00000510658.1:p.Cys504=
ENST00000689002.1:n.588C>T
ENST00000690544.1:c.*807C>T ENSP00000508989.1:n.*807C>T
ENST00000358913.10:c.1536C>T MANE Select ENSP00000351790.5:p.Cys512=
ENST00000354393.6:c.711C>T ENSP00000346369.2:p.Cys237=
ENST00000358913.9:c.1536C>T ENSP00000351790.5:p.Cys512=
ENST00000540630.5:c.1536C>T ENSP00000441668.2:p.Cys512=
ENST00000613327.4:c.654C>T ENSP00000480757.1:p.Cys218=
NM_001256267.1:c.1536C>T NP_001243196.1:p.Cys512=
NM_001256268.1:c.654C>T NP_001243197.1:p.Cys218=
NM_032578.3:c.1536C>T , LRG_410t1:c.1536C>T NP_115967.2:p.Cys512=
NR_045662.3:n.963C>T
NR_045663.3:n.1804C>T
XM_006718043.2:c.1590C>T XP_006718106.1:p.Cys530=
XM_011540292.1:c.1566C>T XP_011538594.1:p.Cys522=
XM_017016833.1:c.1614C>T XP_016872322.1:p.Cys538=
XM_017016834.2:c.1536C>T XP_016872323.1:p.Cys512=
XM_024448236.1:c.414C>T XP_024304004.1:p.Cys138=
NR_045662.4:n.1073C>T
NR_045663.4:n.1749C>T
NM_001256267.2:c.1536C>T NP_001243196.1:p.Cys512=
NM_001256268.2:c.654C>T NP_001243197.1:p.Cys218=
NM_032578.4:c.1536C>T MANE Select NP_115967.2:p.Cys512=