Canonical Allele Identifier: CA5522609
Gene: MYPN HGNC NCBI

Linked Data

dbSNP Id: rs770827738

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68165783G>A , CM000672.2:g.68165783G>A GRCh38
NC_000010.10:g.69925540G>A , CM000672.1:g.69925540G>A GRCh37
NC_000010.9:g.69595546G>A NCBI36
NG_032118.1:g.64667G>A , LRG_410:g.64667G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.740G>A ENSP00000346369.2:p.Gly247Asp
ENST00000373675.4:c.1565G>A ENSP00000362779.4:p.Gly522Asp
ENST00000540630.6:c.1619G>A ENSP00000441668.3:p.Gly540Asp
ENST00000613327.5:c.1565G>A ENSP00000480757.2:p.Gly522Asp
ENST00000687572.1:c.443G>A ENSP00000510427.1:p.Gly148Asp
ENST00000687705.1:c.*1814G>A ENSP00000509639.1:n.*1814G>A
ENST00000688812.1:c.1541G>A ENSP00000510658.1:p.Gly514Asp
ENST00000689002.1:n.617G>A
ENST00000690544.1:c.*836G>A ENSP00000508989.1:n.*836G>A
ENST00000358913.10:c.1565G>A MANE Select ENSP00000351790.5:p.Gly522Asp
ENST00000354393.6:c.740G>A ENSP00000346369.2:p.Gly247Asp
ENST00000358913.9:c.1565G>A ENSP00000351790.5:p.Gly522Asp
ENST00000540630.5:c.1565G>A ENSP00000441668.2:p.Gly522Asp
ENST00000613327.4:c.683G>A ENSP00000480757.1:p.Gly228Asp
NM_001256267.1:c.1565G>A NP_001243196.1:p.Gly522Asp
NM_001256268.1:c.683G>A NP_001243197.1:p.Gly228Asp
NM_032578.3:c.1565G>A , LRG_410t1:c.1565G>A NP_115967.2:p.Gly522Asp
NR_045662.3:n.992G>A
NR_045663.3:n.1833G>A
XM_006718043.2:c.1619G>A XP_006718106.1:p.Gly540Asp
XM_011540292.1:c.1595G>A XP_011538594.1:p.Gly532Asp
XM_017016833.1:c.1643G>A XP_016872322.1:p.Gly548Asp
XM_017016834.2:c.1565G>A XP_016872323.1:p.Gly522Asp
XM_024448236.1:c.443G>A XP_024304004.1:p.Gly148Asp
NR_045662.4:n.1102G>A
NR_045663.4:n.1778G>A
NM_001256267.2:c.1565G>A NP_001243196.1:p.Gly522Asp
NM_001256268.2:c.683G>A NP_001243197.1:p.Gly228Asp
NM_032578.4:c.1565G>A MANE Select NP_115967.2:p.Gly522Asp