Canonical Allele Identifier: CA1917227407
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199464G= , CM000672.2:g.68199464G= GRCh38
NC_000010.10:g.69959221G= , CM000672.1:g.69959221G= GRCh37
NC_000010.9:g.69629227G= NCBI36
NG_032118.1:g.98348G= , LRG_410:g.98348G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2557G= ENSP00000346369.2:p.Val853=
ENST00000540630.6:c.3436G= ENSP00000441668.3:p.Val1146=
ENST00000613327.5:c.3382G= ENSP00000480757.2:p.Val1128=
ENST00000688812.1:c.*645G= ENSP00000510658.1:n.*645G=
ENST00000690544.1:c.*2653G= ENSP00000508989.1:n.*2653G=
ENST00000358913.10:c.3382G= MANE Select ENSP00000351790.5:p.Val1128=
ENST00000354393.6:c.2557G= ENSP00000346369.2:p.Val853=
ENST00000358913.9:c.3382G= ENSP00000351790.5:p.Val1128=
ENST00000540630.5:c.3382G= ENSP00000441668.2:p.Val1128=
ENST00000613327.4:c.2500G= ENSP00000480757.1:p.Val834=
NM_001256267.1:c.3382G= NP_001243196.1:p.Val1128=
NM_001256268.1:c.2500G= NP_001243197.1:p.Val834=
NM_032578.3:c.3382G= , LRG_410t1:c.3382G= NP_115967.2:p.Val1128=
NR_045662.3:n.2809G=
NR_045663.3:n.3511G=
XM_006718043.2:c.3436G= XP_006718106.1:p.Val1146=
XM_011540292.1:c.3412G= XP_011538594.1:p.Val1138=
XR_946029.1:n.1804-189C=
XM_017016833.1:c.3460G= XP_016872322.1:p.Val1154=
XM_017016834.2:c.3382G= XP_016872323.1:p.Val1128=
XM_024448236.1:c.2260G= XP_024304004.1:p.Val754=
NR_045662.4:n.2919G=
NR_045663.4:n.3456G=
NM_001256267.2:c.3382G= NP_001243196.1:p.Val1128=
NM_001256268.2:c.2500G= NP_001243197.1:p.Val834=
NM_032578.4:c.3382G= MANE Select NP_115967.2:p.Val1128=